A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472673



Internal ID21130226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:11666584..11668802hg38UCSC Ensembl
chr12:11819518..11821736hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg382219
hg192219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997160
Samples
Known GenesETV6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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