A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325254



Internal ID20858385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25865043..25865265hg38UCSC Ensembl
chr1:26191534..26191756hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060553
Samples
Known GenesPAQR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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