A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396052



Internal ID21053605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52390051..52395649hg38UCSC Ensembl
chr6:52254849..52260447hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg385599
hg195599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144007
Samples
Known GenesPAQR8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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