A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510616



Internal ID20883936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40452681..40454303hg38UCSC Ensembl
chr15:40744880..40746502hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024199
Samples
Known GenesBAHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510616
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