A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512873



Internal ID20886213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51972651..51975998hg38UCSC Ensembl
chr15:52264848..52268195hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383348
hg193348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2539n223
Supporting Variantsnssv18024044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512873
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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