A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528465



Internal ID15455758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:28353573..28429860hg38UCSC Ensembl
Innerchr12:28506506..28582793hg19UCSC Ensembl
Innerchr12:28397773..28474060hg18UCSC Ensembl
Innerchr12:28397773..28474060hg17UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg3876288
hg1976288
hg1876288
hg1776288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv93n21
Supporting Variantsnssv705067
Samples
Known GenesCCDC91
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528465
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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