A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061455



Internal ID20628495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52293212..52319790hg38UCSC Ensembl
chr1:52758884..52785462hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3826579
hg1926579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335479
Supporting Variants
Samples
Known GenesZFYVE9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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