A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319002



Internal ID20852094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52607713..52617105hg38UCSC Ensembl
chr1:53073385..53082777hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg389393
hg199393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061466
Samples
Known GenesGPX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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