A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328284



Internal ID20861430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90970869..90983728hg38UCSC Ensembl
chr1:91436426..91449285hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3812860
hg1912860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065101
Samples
Known GenesZNF644
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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