A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606524



Internal ID16393933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31123389..31180224hg38UCSC Ensembl
Innerchr7:31163003..31219838hg19UCSC Ensembl
Innerchr7:31129528..31186363hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3856836
hg1956836
hg1856836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154931
SamplesNINDS_13
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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