A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060638



Internal ID20627678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27092530..27100359hg38UCSC Ensembl
chr1:27419021..27426850hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387830
hg197830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324868
Supporting Variants
Samples
Known GenesSLC9A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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