A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135460



Internal ID19276780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360045..39361343hg38UCSC Ensembl
Outerchr13:39934182..39935480hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958n106
Supporting Variantsnssv3989018, nssv3963228
SamplesKWS2, KWS1
Known GenesLHFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135460
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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