A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704980



Internal ID15441632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97952516..98144329hg38UCSC Ensembl
Innerchr4:98873667..99065480hg19UCSC Ensembl
Innerchr4:99092690..99284503hg18UCSC Ensembl
Innerchr4:99230845..99422658hg17UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38191814
hg19191814
hg18191814
hg17191814
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528390
Supporting Variants
Samples
Known GenesSTPG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704980
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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