A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035773



Internal ID21945116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8634007..8634067hg38UCSC Ensembl
chr12:8786603..8786663hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035773
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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