A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982569



Internal ID18879181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13115031..13115096hg38UCSC Ensembl
Outerchr10:13157031..13157096hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145432
Supporting Variants
SamplesKWS1
Known GenesOPTN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982569
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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