A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608993



Internal ID16049716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150856387..150863234hg38UCSC Ensembl
Innerchr7:150553475..150560322hg19UCSC Ensembl
Innerchr7:150184408..150191255hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386848
hg196848
hg186848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099482, nssv1099480, nssv1099483, nssv1099481
Samples
Known GenesAOC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608993
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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