A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499906



Internal ID20873131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21006901..21055938hg38UCSC Ensembl
chr16:21018223..21067259hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3849038
hg1949037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028823
Samples
Known GenesDNAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499906
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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