A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333413



Internal ID20866589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227655701..227656900hg38UCSC Ensembl
chr1:227843402..227844601hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058236
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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