A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139555



Internal ID18918159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:96695598..96695692hg38UCSC Ensembl
Outerchr13:97347852..97347946hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1017n106
Supporting Variantsnssv3977141
SamplesKWS1
Known GenesHS6ST3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139555
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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