A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030141



Internal ID18772672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52748106..52827956hg38UCSC Ensembl
Innerchr6:52612904..52692754hg19UCSC Ensembl
Innerchr6:52720863..52800713hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3879851
hg1979851
hg1879851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5961n100
Supporting Variantsnssv3745485, nssv3657460, nssv3745483, nssv3745484
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030141
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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