A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654496



Internal ID18952777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160604003..160647502hg38UCSC Ensembl
Innerchr6:161025035..161068534hg19UCSC Ensembl
Innerchr6:160945025..160988524hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3843500
hg1943500
hg1843500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033354
Supporting Variants
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)nssv3654496
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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