A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445648



Internal ID21103201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91177645..91181925hg38UCSC Ensembl
chr10:92937402..92941682hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg384281
hg194281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985330
Samples
Known GenesPCGF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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