A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765785



Internal ID19314242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113584384..113585385hg38UCSC Ensembl
chr13:114238699..114239700hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071131
Supporting Variants
SamplesKWP1
Known GenesTFDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765785
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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