A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500761



Internal ID18741716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108937747..108955511hg38UCSC Ensembl
Innerchr1:109480369..109498133hg19UCSC Ensembl
Innerchr1:109281892..109299656hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817765
hg1917765
hg1817765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000677
Supporting Variants
Samples
Known GenesCLCC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3500761
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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