A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515554



Internal ID20888914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4431725..4484226hg38UCSC Ensembl
chr16:4481726..4534227hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3852502
hg1952502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029648
Samples
Known GenesDNAJA3, HMOX2, NMRAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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