A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325702



Internal ID20858833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172652227..172652731hg38UCSC Ensembl
chr1:172621367..172621871hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38505
hg19505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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