A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518795



Internal ID18470390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:116327708..116367310hg38UCSC Ensembl
Innerchr10:118087220..118126822hg19UCSC Ensembl
Innerchr10:118077210..118116812hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3839603
hg1939603
hg1839603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047591
Supporting Variants
Samples
Known GenesCCDC172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518795
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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