A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324000



Internal ID20857123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53069706..53073488hg38UCSC Ensembl
chr1:53535378..53539160hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383783
hg193783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061490
Samples
Known GenesPODN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324000
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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