A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323748



Internal ID20856870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222721301..222723000hg38UCSC Ensembl
chr1:222894643..222896342hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058694
Samples
Known GenesBROX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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