A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516712



Internal ID15444005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155763820..155776126hg38UCSC Ensembl
Innerchr3:155481609..155493915hg19UCSC Ensembl
Innerchr3:156964303..156976609hg18UCSC Ensembl
Innerchr3:156964311..156976617hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3812307
hg1912307
hg1812307
hg1712307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689245, nssv680295, nssv676694, nssv656615, nssv670320, nssv671193
Samples
Known GenesC3orf33
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516712
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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