A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523176



Internal ID15450469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155382849..155389631hg38UCSC Ensembl
Innerchr7:155175544..155182326hg19UCSC Ensembl
Innerchr7:154868305..154875087hg18UCSC Ensembl
Innerchr7:154675020..154681802hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg386783
hg196783
hg186783
hg176783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698889
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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