A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501993



Internal ID20875233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4380010..4408838hg38UCSC Ensembl
chr16:4430011..4458839hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3828829
hg1928829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029641
Samples
Known GenesCORO7, CORO7-PAM16, VASN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501993
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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