A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031938



Internal ID18774472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26466954..26501669hg38UCSC Ensembl
Innerchr6:26467182..26501897hg19UCSC Ensembl
Innerchr6:26575161..26609876hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3834716
hg1934716
hg1834716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654859
Samples
Known GenesBTN1A1, BTN2A1, LOC285819
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031938
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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