A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505907



Internal ID20879181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78532293..78543984hg38UCSC Ensembl
chr15:78824635..78836326hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3811692
hg1911692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026770
Samples
Known GenesHYKK, PSMA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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