A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668777



Internal ID15405429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:141097310..141100771hg38UCSC Ensembl
Innerchr5:140476894..140480355hg19UCSC Ensembl
Innerchr5:140457078..140460539hg18UCSC Ensembl
Innerchr5:140457078..140460539hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg383462
hg193462
hg183462
hg173462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516514
Supporting Variants
Samples
Known GenesPCDHB2, PCDHB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668777
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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