A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020677



Internal ID19109896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:62201679..62599758hg38UCSC Ensembl
Innerchr6:62911584..63309663hg19UCSC Ensembl
Innerchr6:62969543..63367622hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38398080
hg19398080
hg18398080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5994n100
Supporting Variantsnssv3657640
Samples
Known GenesKHDRBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020677
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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