A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515356



Internal ID20888715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81139892..81236510hg38UCSC Ensembl
chr16:81173497..81270115hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3896619
hg1996619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2947n223
Supporting Variantsnssv18032819
Samples
Known GenesPKD1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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