A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766167



Internal ID19312867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37784827..37788028hg38UCSC Ensembl
chr1:38250499..38253700hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078330
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766167
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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