A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140117



Internal ID19247855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125748900..125748963hg38UCSC Ensembl
Outerchr10:127437469..127437532hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978829
SamplesKWS2
Known GenesC10orf137
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140117
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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