A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120676



Internal ID19265886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:39360094..39361339hg38UCSC Ensembl
Outerchr13:39934231..39935476hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv958n106
Supporting Variantsnssv3963107
SamplesKWS2
Known GenesLHFP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120676
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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