A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955116



Internal ID18878531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:32949940..32950066hg38UCSC Ensembl
Outerchr15:33242141..33242267hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127421
Supporting Variants
SamplesKWS1
Known GenesFMN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955116
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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