A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019558



Internal ID19108776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142800440..142833417hg38UCSC Ensembl
Innerchr6:143121577..143154554hg19UCSC Ensembl
Innerchr6:143163270..143196247hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3832978
hg1932978
hg1832978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654451
Samples
Known GenesHIVEP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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