A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128708



Internal ID18938014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802527..113803627hg38UCSC Ensembl
Outerchr13:114505500..114506600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1045n106
Supporting Variantsnssv3960621
SamplesKWS1
Known GenesTMEM255B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128708
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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