A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607774



Internal ID16395183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89928234..90080467hg38UCSC Ensembl
Innerchr7:89557548..89709781hg19UCSC Ensembl
Innerchr7:89395484..89547717hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38152234
hg19152234
hg18152234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11496n54
Supporting Variantsnssv1155361, nssv1155360
SamplesNINDS_193, NINDS_149
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607774
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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