A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003881



Internal ID19188698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133203100..133203252hg38UCSC Ensembl
Outerchr10:135016604..135016756hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151318
Supporting Variants
SamplesKWB1
Known GenesKNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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