A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435922



Internal ID21093475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5769409..5770691hg38UCSC Ensembl
chr10:5811372..5812654hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983074
Samples
Known GenesGDI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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