A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528932



Internal ID15456225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91097000..91128921hg38UCSC Ensembl
Innerchr7:90726315..90758236hg19UCSC Ensembl
Innerchr7:90564251..90596172hg18UCSC Ensembl
Innerchr7:90370966..90402887hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3831922
hg1931922
hg1831922
hg1731922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705623
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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