A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501185



Internal ID20874416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10296842..10331946hg38UCSC Ensembl
chr16:10390699..10425803hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3835105
hg1935105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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