A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495613



Internal ID20868807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74638101..74638900hg38UCSC Ensembl
chr16:74671999..74672798hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031428
Samples
Known GenesRFWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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