A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327714



Internal ID20860855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62332737..62335171hg38UCSC Ensembl
chr1:62798408..62800842hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382435
hg192435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327714
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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