A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513516



Internal ID20886861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57770298..57771686hg38UCSC Ensembl
chr15:58062496..58063884hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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