A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655238



Internal ID18953519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90688742..90857507hg38UCSC Ensembl
Innerchr7:90318056..90486822hg19UCSC Ensembl
Innerchr7:90155992..90324758hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38168766
hg19168767
hg18168767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020637
Supporting Variants
Samples
Known GenesCDK14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655238
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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