A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735940



Internal ID20511883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30056359..30062451hg38UCSC Ensembl
chr12:30209292..30215384hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg386093
hg196093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735940
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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