A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528432



Internal ID15109039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35991094..36067577hg38UCSC Ensembl
Innerchr6:35958871..36035354hg19UCSC Ensembl
Innerchr6:36066849..36143332hg18UCSC Ensembl
Innerchr6:36066849..36143332hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3876484
hg1976484
hg1876484
hg1776484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705025
Samples
Known GenesMAPK14, SLC26A8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528432
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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