A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980698



Internal ID18872281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13347400..13348100hg38UCSC Ensembl
Outerchr10:13389400..13390100hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143493
Supporting Variants
SamplesKWS1
Known GenesSEPHS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980698
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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