A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326421



Internal ID20859556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44103235..44107156hg38UCSC Ensembl
chr1:44568907..44572828hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg383922
hg193922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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