A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500282



Internal ID20873507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85702641..85769286hg38UCSC Ensembl
chr16:85736247..85802892hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3866646
hg1966646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033404
Samples
Known GenesC16orf74, MIR1910, MIR7851
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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