A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334043



Internal ID20867224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77798063..77842264hg38UCSC Ensembl
chr1:78263748..78307949hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3844202
hg1944202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063227
Samples
Known GenesFAM73A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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