A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330893



Internal ID20864051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61799198..61800031hg38UCSC Ensembl
chr1:62264870..62265703hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062162
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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