A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321275



Internal ID20854378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39120171..39122472hg38UCSC Ensembl
chr1:39585843..39588144hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060091
Samples
Known GenesMACF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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