A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152639



Internal ID19201318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98918332..98932574hg38UCSC Ensembl
Outerchr10:100678089..100692331hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3814243
hg1914243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999820
SamplesKWB1
Known GenesHPSE2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152639
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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