A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324520



Internal ID20857648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29703896..29705713hg38UCSC Ensembl
chr1:30176743..30178560hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381818
hg191818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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