A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770484



Internal ID19309653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37752527..37753628hg38UCSC Ensembl
chr1:38218199..38219300hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078328
Supporting Variants
SamplesKWP1
Known GenesEPHA10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770484
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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