A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499172



Internal ID20872389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75674178..75689547hg38UCSC Ensembl
chr16:75708076..75723445hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3815370
hg1915370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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