A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990477



Internal ID18880057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99814606..99814684hg38UCSC Ensembl
Outerchr10:101574363..101574441hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137953
Supporting Variants
SamplesKWS2
Known GenesABCC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990477
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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