A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335417



Internal ID20868609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10483318..10484378hg38UCSC Ensembl
chr1:10543375..10544435hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381061
hg191061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050377
Samples
Known GenesPEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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