A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144614



Internal ID18914276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1495621..1495706hg38UCSC Ensembl
Outerchr10:1537816..1537901hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv336n106
Supporting Variantsnssv3995466
SamplesKWS1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144614
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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