A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459518



Internal ID21117071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9112275..9112924hg38UCSC Ensembl
chr12:9264871..9265520hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005587
Samples
Known GenesA2M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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