A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320977



Internal ID20854078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62833673..62846511hg38UCSC Ensembl
chr1:63299344..63312182hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3812839
hg1912839
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062244
Samples
Known GenesATG4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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