A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508249



Internal ID20881548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41920634..41930628hg38UCSC Ensembl
chr15:42212832..42222826hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg389995
hg199995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023915
Samples
Known GenesEHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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