A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062642



Internal ID20629682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66987881..66988339hg38UCSC Ensembl
chr1:67453564..67454022hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327660
Supporting Variants
Samples
Known GenesMIER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00077


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