A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454788



Internal ID21112341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45648189..45656373hg38UCSC Ensembl
chr10:46143637..46151821hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388185
hg198185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980421
Samples
Known GenesZFAND4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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