A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704620



Internal ID15441272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48385834..48411902hg38UCSC Ensembl
Innerchr4:48387851..48413919hg19UCSC Ensembl
Innerchr4:48082608..48108676hg18UCSC Ensembl
Innerchr4:48228779..48254847hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3826069
hg1926069
hg1826069
hg1726069
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528084
Supporting Variants
Samples
Known GenesSLAIN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704620
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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