A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763998



Internal ID19313285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24076629..24077130hg38UCSC Ensembl
chr2:24299499..24300000hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072930
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763998
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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