A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999644



Internal ID19186795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35742836..35742932hg38UCSC Ensembl
Outerchr10:36031764..36031860hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146443
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999644
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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