A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325890



Internal ID20859023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227673054..227673660hg38UCSC Ensembl
chr1:227860755..227861361hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058239
Samples
Known GenesZNF678
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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