A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744704



Internal ID16038660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21627539..21773800hg38UCSC Ensembl
Innerchr10:21916468..22062729hg19UCSC Ensembl
Innerchr10:21956474..22102735hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38146262
hg19146262
hg18146262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550203
Supporting Variants
Samples
Known GenesDNAJC1, MLLT10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744704
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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