A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325132



Internal ID20858262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67698201..67700300hg38UCSC Ensembl
chr1:68163884..68165983hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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