A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508632



Internal ID20881936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23737666..23783955hg38UCSC Ensembl
chr16:23748987..23795276hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3846290
hg1946290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029425
Samples
Known GenesCHP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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