A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977221



Internal ID19240118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83385548..83393248hg38UCSC Ensembl
Outerchr15:84054300..84062000hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387701
hg197701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139635
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977221
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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