A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126339



Internal ID18929716
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 StatusM
Merged Variantsdgv922n106
Supporting Variantsnssv3984579
SamplesKWS1
Known GenesIL17D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126339
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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