A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330034



Internal ID20863188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27120344..27125756hg38UCSC Ensembl
chr1:27446835..27452247hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385413
hg195413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060639
Samples
Known GenesSLC9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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