A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510414



Internal ID20883732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75589089..75613246hg38UCSC Ensembl
chr16:75622987..75647144hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824158
hg1924158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032728
Samples
Known GenesADAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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