A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011085



Internal ID22072716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51973538..51981087hg38UCSC Ensembl
Outerchr15:51970414..51983058hg38UCSC Ensembl
Innerchr15:52265735..52273284hg19UCSC Ensembl
Outerchr15:52262611..52275255hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3812645
hg1912645
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155178
Supporting Variants
Samples
Known GenesLEO1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011085
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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