A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770274



Internal ID19313469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8627004..8627071hg38UCSC Ensembl
chr2:8767134..8767201hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071573
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770274
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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