A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003058



Internal ID18841569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1439509..1439593hg38UCSC Ensembl
Outerchr10:1481704..1481788hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151635
Supporting Variants
SamplesKWB1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003058
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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