A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989807



Internal ID18879993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82358484..82446454hg38UCSC Ensembl
Outerchr15:82650700..82738600hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3887971
hg1987901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136198
Supporting Variants
SamplesKWS2
Known GenesGOLGA6L20, GOLGA6L9, UBE2Q2P2, UBE2Q2P3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989807
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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