A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137928



Internal ID19268140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:59644646..59644716hg38UCSC Ensembl
Outerchr10:61404404..61404474hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968212, nssv3985466
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137928
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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