A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492217



Internal ID21149770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122414742..122442488hg38UCSC Ensembl
chr12:122899289..122927035hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3827747
hg1927747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998703
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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