A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684338



Internal ID15074304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:807215..1386951hg38UCSC Ensembl
Innerchr3:848898..1428635hg19UCSC Ensembl
Innerchr3:823898..1403635hg18UCSC Ensembl
Innerchr3:823898..1403635hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38579737
hg19579738
hg18579738
hg17579738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known GenesCNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684338
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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