A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498131



Internal ID20871339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58645001..58646700hg38UCSC Ensembl
chr15:58937200..58938899hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026184
Samples
Known GenesADAM10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498131
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