A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328628



Internal ID20861776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9833058..9838221hg38UCSC Ensembl
chr1:9893116..9898279hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385164
hg195164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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