A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328216



Internal ID20861361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62139295..62145783hg38UCSC Ensembl
chr1:62604967..62611455hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg386489
hg196489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063405
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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