A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984579



Internal ID18879095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:20703761..20704461hg38UCSC Ensembl
Outerchr13:21277900..21278600hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126339
Supporting Variants
SamplesKWS1
Known GenesIL17D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984579
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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