A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510796



Internal ID20884119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84802888..84998209hg38UCSC Ensembl
chr16:84836494..85031815hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38195322
hg19195322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178445
Samples
Known GenesCRISPLD2, ZDHHC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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