A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327289



Internal ID20860426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223237901..223240000hg38UCSC Ensembl
chr1:223411243..223413342hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057662
Samples
Known GenesSUSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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