A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698660



Internal ID15435312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227102438..227115211hg38UCSC Ensembl
Innerchr1:227290139..227302912hg19UCSC Ensembl
Innerchr1:225356762..225369535hg18UCSC Ensembl
Innerchr1:223596874..223609647hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3812774
hg1912774
hg1812774
hg1712774
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522990
Supporting Variants
Samples
Known GenesCDC42BPA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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