A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674906



Internal ID15064872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1324656..1324874hg38UCSC Ensembl
Innerchr3:1366340..1366558hg19UCSC Ensembl
Innerchr3:1341340..1341558hg18UCSC Ensembl
Innerchr3:1341340..1341558hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38219
hg19219
hg18219
hg17219
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
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)nssv674906
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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