A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998305



Internal ID18843715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103337763..103338076hg38UCSC Ensembl
Outerchr10:105097520..105097833hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146943
Supporting Variants
SamplesKWB1
Known GenesPCGF6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998305
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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