A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111655



Internal ID19273079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:72319511..72324303hg38UCSC Ensembl
Outerchr13:72893649..72898441hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg384793
hg194793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv996n106
Supporting Variantsnssv3964552
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111655
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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