A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505145



Internal ID20878411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53448601..53560600hg38UCSC Ensembl
chr15:53740798..53852797hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38112000
hg19112000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025985
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505145
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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