A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017944



Internal ID19107161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:121279392..121323216hg38UCSC Ensembl
Innerchr6:121600538..121644362hg19UCSC Ensembl
Innerchr6:121642237..121686061hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3843825
hg1943825
hg1843825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654340
Samples
Known GenesTBC1D32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017944
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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