A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022275



Internal ID19111493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160610658..160647531hg38UCSC Ensembl
Innerchr6:161031690..161068563hg19UCSC Ensembl
Innerchr6:160951680..160988553hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3836874
hg1936874
hg1836874
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654502, nssv3654503
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)nsv1022275
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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