A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323053



Internal ID20856168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117818406..117819884hg38UCSC Ensembl
chr1:118361028..118362506hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323053
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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