A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499230



Internal ID20872448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53470924..53777260hg38UCSC Ensembl
chr15:53763121..54069457hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38306337
hg19306337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025988
Samples
Known GenesWDR72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer