A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512118



Internal ID20885448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63736901..63740300hg38UCSC Ensembl
chr15:64029100..64032499hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025640
Samples
Known GenesHERC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512118
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