A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328719



Internal ID20861868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161220385..161221038hg38UCSC Ensembl
chr1:161190175..161190828hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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