A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609170



Internal ID16396579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156438411..156446434hg38UCSC Ensembl
Innerchr7:156231105..156239128hg19UCSC Ensembl
Innerchr7:155923866..155931889hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388024
hg198024
hg188024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155931
Samples1780846322_A
Known GenesLOC285889
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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