A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137920



Internal ID18905561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:48709111..48709434hg38UCSC Ensembl
Outerchr10:49917156..49917479hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv453n106
Supporting Variantsnssv3962164, nssv3968204
SamplesKWS2, KWS1
Known GenesWDFY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137920
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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