A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073375



Internal ID18979385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19197747..19198023hg38UCSC Ensembl
chr8:19055257..19055533hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770107
SamplesKWP1
Known GenesLOC100128993
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073375
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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