A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335092



Internal ID20868283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226855901..226859800hg38UCSC Ensembl
chr1:227043602..227047501hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg383900
hg193900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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