A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022089



Internal ID18764623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31416071..31498018hg38UCSC Ensembl
Innerchr6:31383848..31465795hg19UCSC Ensembl
Innerchr6:31491827..31573774hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3881948
hg1981948
hg1881948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5944n100
Supporting Variantsnssv3655890
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)nsv1022089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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