A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513318



Internal ID20886661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75572231..75574325hg38UCSC Ensembl
chr16:75606129..75608223hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg382095
hg192095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032726
Samples
Known GenesGABARAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513318
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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