A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021984



Internal ID18764518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392318..31497326hg38UCSC Ensembl
Innerchr6:31360095..31465103hg19UCSC Ensembl
Innerchr6:31468074..31573082hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38105009
hg19105009
hg18105009
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5943n100
Supporting Variantsnssv3655859, nssv3655855, nssv3655863, nssv3655857, nssv3655861, nssv3655858, nssv3655862, nssv3745371, nssv3655860, nssv3655856
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021984
Frequency
Sample Size29084
Observed Gain3
Observed Loss7
Observed Complex0
Frequencyn/a


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