A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122791



Internal ID18901619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:18855356..18855418hg38UCSC Ensembl
Outerchr13:19429496..19429558hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971377
SamplesKWS2
Known GenesANKRD20A9P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122791
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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