A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705367



Internal ID15442019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:166803447..166817313hg38UCSC Ensembl
Innerchr4:167724598..167738464hg19UCSC Ensembl
Innerchr4:167961173..167975039hg18UCSC Ensembl
Innerchr4:168099328..168113194hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813867
hg1913867
hg1813867
hg1713867
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528717
Supporting Variants
Samples
Known GenesSPOCK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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