A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506531



Internal ID20879812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1836490..1836796hg38UCSC Ensembl
chr16:1886491..1886797hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028108
Samples
Known GenesFAHD1, MEIOB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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