A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326325



Internal ID20859460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:176484998..176485555hg38UCSC Ensembl
chr1:176454134..176454691hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053741
Samples
Known GenesPAPPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326325
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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