A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513312



Internal ID20886655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23613344..23620833hg38UCSC Ensembl
chr16:23624665..23632154hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg387490
hg197490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029419
Samples
Known GenesPALB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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