A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4002203



Internal ID19186923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:106190949..106191848hg38UCSC Ensembl
Outerchr10:107950707..107951606hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153552
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4002203
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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