A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001463



Internal ID19187771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:7564636..7565937hg38UCSC Ensembl
Outerchr10:7606599..7607900hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147953
Supporting Variants
SamplesKWB1
Known GenesITIH5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001463
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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