A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984491



Internal ID19207651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:68827243..68828443hg38UCSC Ensembl
Outerchr10:70587000..70588200hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126258
Supporting Variants
SamplesKWS1
Known GenesSTOX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984491
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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