A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441723



Internal ID21099276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51911721..51917456hg38UCSC Ensembl
chr10:53671481..53677216hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385736
hg195736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981625
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441723
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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