A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136199



Internal ID19269221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82360382..82453704hg38UCSC Ensembl
Outerchr15:83028100..83122400hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3893323
hg1994301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1254n106
Supporting Variantsnssv3989808
SamplesKWS2
Known GenesGOLGA6L20, GOLGA6L9, UBE2Q2P2, UBE2Q2P3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136199
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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