A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956619



Internal ID17305492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:37742563..37742730hg38UCSC Ensembl
Outerchr1:38208235..38208402hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000471
SamplesBILGI_BIOE
Known GenesEPHA10
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956619
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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