A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506405



Internal ID20879684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77349011..77661485hg38UCSC Ensembl
chr16:77382908..77695382hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38312475
hg19312475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032008
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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