A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325327



Internal ID20858458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158971682..158972324hg38UCSC Ensembl
chr1:158941472..158942114hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38643
hg19643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053478
Samples
Known GenesPYHIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325327
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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