A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116983



Internal ID18925993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48709177..48709431hg38UCSC Ensembl
Outerchr10:49917222..49917476hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv453n106
Supporting Variantsnssv3956585
SamplesKWS1
Known GenesWDFY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116983
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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