A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332331



Internal ID20865501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184943523..184991825hg38UCSC Ensembl
chr1:184912655..184960957hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3848303
hg1948303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054451
Samples
Known GenesFAM129A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332331
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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