A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765961



Internal ID18967388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33015961..33016662hg38UCSC Ensembl
chr13:33590099..33590800hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071091
Supporting Variants
SamplesKWP1
Known GenesKL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765961
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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