A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15313627



Internal ID5315443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84600461..84697551hg38UCSC Ensembl
chr15:85143692..85240782hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3897091
hg1997091
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637095
Supporting Variants
SamplesHG02885
Known GenesNMB, SCAND2P, SEC11A, WDR73, ZSCAN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15313627
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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