A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978846



Internal ID19245877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74472565..74472627hg38UCSC Ensembl
Outerchr15:74764906..74764968hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140134
Supporting Variants
SamplesKWS2
Known GenesUBL7-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978846
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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