A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995274



Internal ID19221797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:38270378..38270461hg38UCSC Ensembl
Outerchr10:38559306..38559389hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144471
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3995274
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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