A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705706



Internal ID15442358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83092451..83195095hg38UCSC Ensembl
Innerchr3:83141602..83244246hg19UCSC Ensembl
Innerchr3:83224292..83326936hg18UCSC Ensembl
Innerchr3:83224292..83326936hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38102645
hg19102645
hg18102645
hg17102645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529000
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705706
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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