A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968204



Internal ID18890735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48709111..48709434hg38UCSC Ensembl
Outerchr10:49917156..49917479hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1137920
Supporting Variants
SamplesKWS2
Known GenesWDFY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968204
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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