A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143627



Internal ID19260493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28667871..28669771hg38UCSC Ensembl
Outerchr10:28956800..28958700hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994313
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143627
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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