A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521174



Internal ID15448467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:155687239..155706412hg38UCSC Ensembl
Innerchr6:156008373..156027546hg19UCSC Ensembl
Innerchr6:156050065..156069238hg18UCSC Ensembl
Innerchr6:156100486..156119659hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3819174
hg1919174
hg1819174
hg1719174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686510, nssv683811
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521174
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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