A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987189



Internal ID18876821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84218048..84225448hg38UCSC Ensembl
Outerchr15:84886800..84894200hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387401
hg197401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132414
Supporting Variants
SamplesKWS1
Known GenesLOC388152
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987189
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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