A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512486



Internal ID20885820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75895743..76702368hg38UCSC Ensembl
chr16:75929641..76736265hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38806626
hg19806625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190155
Samples
Known GenesCNTNAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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