A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118477



Internal ID18923030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46163664..46283064hg38UCSC Ensembl
Outerchr10:47534900..47654300hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119401
hg19119401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958985
SamplesKWS1
Known GenesANTXRLP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118477
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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