A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030802



Internal ID18773333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31394533..31481492hg38UCSC Ensembl
Innerchr6:31362310..31449269hg19UCSC Ensembl
Innerchr6:31470289..31557248hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3886960
hg1986960
hg1886960
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745372
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)nsv1030802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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