A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3463766



Internal ID18713650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16855930..16931176hg38UCSC Ensembl
Innerchr1:17182425..17257671hg19UCSC Ensembl
Innerchr1:17055012..17130258hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3875247
hg1975247
hg1875247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013701
Supporting Variants
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3463766
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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