A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497329



Internal ID20870535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13923101..13929600hg38UCSC Ensembl
chr16:14016958..14023457hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028438
Samples
Known GenesERCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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