A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771886



Internal ID18967727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96695505..96695681hg38UCSC Ensembl
chr13:97347759..97347935hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070189
Supporting Variants
SamplesKWP1
Known GenesHS6ST3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771886
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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