A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730736



Internal ID20506650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97578337..97578411hg38UCSC Ensembl
chr10:99338094..99338168hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282980
Samples
Known GenesANKRD2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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