A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326976



Internal ID20860113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23312439..23313061hg38UCSC Ensembl
chr1:23638932..23639554hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058784
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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