A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699337



Internal ID15435989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12053630..12075120hg38UCSC Ensembl
Innerchr3:12095130..12116620hg19UCSC Ensembl
Innerchr3:12070130..12091620hg18UCSC Ensembl
Innerchr3:12070130..12091620hg17UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3821491
hg1921491
hg1821491
hg1721491
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519277
Supporting Variants
Samples
Known GenesSYN2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699337
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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