A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509438



Internal ID20882747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1593456..1605491hg38UCSC Ensembl
chr16:1643457..1655492hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812036
hg1912036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028522
Samples
Known GenesIFT140
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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