A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139519



Internal ID19268097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35475572..35479672hg38UCSC Ensembl
Outerchr10:35764500..35768600hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977107
SamplesKWS2
Known GenesCCNY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139519
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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