A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124610



Internal ID19262324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1767006..1770606hg38UCSC Ensembl
Outerchr10:1809200..1812800hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383601
hg193601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3976664
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124610
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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