A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332944



Internal ID20866119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32007594..32010102hg38UCSC Ensembl
chr1:32473195..32475703hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382509
hg192509
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332944
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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