A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325590



Internal ID20858721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10461141..10462058hg38UCSC Ensembl
chr1:10521198..10522115hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050351
Samples
Known GenesDFFA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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