A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761925



Internal ID15709195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132139965..132247418hg38UCSC Ensembl
Innerchr10:133953469..134060922hg19UCSC Ensembl
Innerchr10:133803459..133910912hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38107454
hg19107454
hg18107454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552502
Supporting Variants
Samples
Known GenesDPYSL4, JAKMIP3, STK32C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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