A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441571



Internal ID21099124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:51599401..51600700hg38UCSC Ensembl
chr10:53359161..53360460hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981599
Samples
Known GenesPRKG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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