A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462607



Internal ID21120160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25590144..25591138hg38UCSC Ensembl
chr12:25743078..25744072hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180392
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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