A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505987



Internal ID20879262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61876901..61878200hg38UCSC Ensembl
chr15:62169100..62170399hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026125
Samples
Known GenesVPS13C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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