A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324526



Internal ID20857654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60323243..60324345hg38UCSC Ensembl
chr1:60788915..60790017hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg381103
hg191103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324526
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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