A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025876



Internal ID18768408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31420646..31492443hg38UCSC Ensembl
Innerchr6:31388423..31460220hg19UCSC Ensembl
Innerchr6:31496402..31568199hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3871798
hg1971798
hg1871798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5944n100
Supporting Variantsnssv3655895, nssv3655896
Samples
Known GenesHCG26, HCP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025876
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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