A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507934



Internal ID20881230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56692001..56692900hg38UCSC Ensembl
chr15:56984199..56985098hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025245
Samples
Known GenesZNF280D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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