A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026947



Internal ID19116165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68192897..68224756hg38UCSC Ensembl
Innerchr6:68902789..68934648hg19UCSC Ensembl
Innerchr6:68959510..68991369hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3831860
hg1931860
hg1831860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747077
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026947
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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