A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763667



Internal ID18958877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159971792..159972693hg38UCSC Ensembl
chr5:159398799..159399700hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074340
Supporting Variants
SamplesKWP1
Known GenesADRA1B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763667
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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