A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745477



Internal ID19043758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:38364592..38486751hg38UCSC Ensembl
Innerchr6:38332368..38454527hg19UCSC Ensembl
Innerchr6:38440346..38562505hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38122160
hg19122160
hg18122160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022724
Supporting Variants
Samples
Known GenesBTBD9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3745477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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