A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135764



Internal ID18921845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1547614..1547753hg38UCSC Ensembl
Outerchr10:1589809..1589948hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv337n106
Supporting Variantsnssv3989351
SamplesKWS2
Known GenesADARB2, ADARB2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135764
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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