A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499626



Internal ID20872848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86516407..86546812hg38UCSC Ensembl
chr16:86550013..86580418hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3830406
hg1930406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033491
Samples
Known GenesMTHFSD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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