A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513122



Internal ID20886462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:46152834..46219414hg38UCSC Ensembl
chr15:46445032..46511612hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3866581
hg1966581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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