A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990962



Internal ID19234579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85896814..85896904hg38UCSC Ensembl
Outerchr15:86440045..86440135hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138393
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990962
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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