A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328775



Internal ID20861925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22587296..22671210hg38UCSC Ensembl
chr1:22913789..22997703hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3883915
hg1983915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058384
Samples
Known GenesC1QA, C1QB, C1QC, EPHA8, MIR6127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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