A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137492



Internal ID19270210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98269096..98269225hg38UCSC Ensembl
Outerchr10:100028853..100028982hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976937
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137492
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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