A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607783



Internal ID16395192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90181390..90183138hg38UCSC Ensembl
Innerchr7:89810704..89812452hg19UCSC Ensembl
Innerchr7:89648640..89650388hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg381749
hg191749
hg181749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11497n54
Supporting Variantsnssv1090143, nssv1090128, nssv1090122, nssv1090129, nssv1090123, nssv1090145, nssv1090114, nssv1090111, nssv1090148, nssv1090141, nssv1090124, nssv1090142, nssv1090146, nssv1090125, nssv1090130, nssv1090137, nssv1090118, nssv1090134, nssv1090121, nssv1090161, nssv1090110, nssv1090162, nssv1090135, nssv1090113, nssv1090116, nssv1090126, nssv1090159, nssv1090158, nssv1090151, nssv1090147, nssv1090127, nssv1090153, nssv1090156, nssv1090144, nssv1090108, nssv1090112, nssv1090150, nssv1090115, nssv1090164, nssv1090166, nssv1090138, nssv1090136, nssv1090152, nssv1090132, nssv1090139, nssv1090119, nssv1090131, nssv1090117, nssv1090120, nssv1090167, nssv1090168, nssv1090157, nssv1090140, nssv1090163, nssv1090155, nssv1090154, nssv1090133, nssv1090160, nssv1090165, nssv1090149, nssv1090109
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607783
Frequency
Sample Size17421
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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