A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978545



Internal ID19247191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92571382..92571471hg38UCSC Ensembl
Outerchr15:93114612..93114701hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115983
Supporting Variants
SamplesKWS2
Known GenesLINC00930
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978545
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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