A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328558



Internal ID20861706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73102631..73256201hg38UCSC Ensembl
chr1:73568314..73721884hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38153571
hg19153571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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