A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746757



Internal ID20522771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126200779..126200856hg38UCSC Ensembl
chr10:127889348..127889425hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290540
Samples
Known GenesADAM12
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746757
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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