A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710526



Internal ID15657796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15683620..15684581hg38UCSC Ensembl
Innerchr1:16010115..16011076hg19UCSC Ensembl
Innerchr1:15882702..15883663hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38962
hg19962
hg18962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545606
Supporting Variants
Samples
Known GenesPLEKHM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710526
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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