A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710895



Internal ID15658165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16856620..16955930hg38UCSC Ensembl
Innerchr1:17183115..17282425hg19UCSC Ensembl
Innerchr1:17055702..17155012hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3899311
hg1999311
hg1899311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545671
Supporting Variants
Samples
Known GenesCROCC, MIR3675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710895
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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