A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003598



Internal ID19190168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14894355..14894665hg38UCSC Ensembl
Outerchr10:14936354..14936664hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150299
Supporting Variants
SamplesKWB1
Known GenesSUV39H2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003598
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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