A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332882



Internal ID20866057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52155289..52156838hg38UCSC Ensembl
chr1:52620961..52622510hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062028
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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