A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486607



Internal ID21144160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120273243..120285500hg38UCSC Ensembl
chr12:120711046..120723303hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3812258
hg1912258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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