A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326833



Internal ID20859970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50959601..50960200hg38UCSC Ensembl
chr1:51425273..51425872hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060921
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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