A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321016



Internal ID20854118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60717755..60718275hg38UCSC Ensembl
chr1:61183427..61183947hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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