A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321419



Internal ID20854524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47559493..47561432hg38UCSC Ensembl
chr1:48025165..48027104hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381940
hg191940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321419
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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