A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767151



Internal ID19313768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34038698..34039199hg38UCSC Ensembl
chr15:34330899..34331400hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069850
Supporting Variants
SamplesKWP1
Known GenesAVEN, CHRM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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