A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999844



Internal ID20566884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25544003..25544420hg38UCSC Ensembl
chr12:25696937..25697354hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457830
Supporting Variants
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00209


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