A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332635



Internal ID20865808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:119804862..119805823hg38UCSC Ensembl
chr1:120347485..120348446hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051283
Samples
Known GenesREG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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