A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025771



Internal ID19114988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160610658..160647923hg38UCSC Ensembl
Innerchr6:161031690..161068955hg19UCSC Ensembl
Innerchr6:160951680..160988945hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3837266
hg1937266
hg1837266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6167n100
Supporting Variantsnssv3654505
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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