A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508762



Internal ID20882066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87251853..87309372hg38UCSC Ensembl
chr16:87285459..87342978hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3857520
hg1957520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2959n223
Supporting Variantsnssv18033608
Samples
Known GenesC16orf95, LOC101928682
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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