A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051163



Internal ID20618203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10946413..10947377hg38UCSC Ensembl
chr1:11006470..11007434hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327365
Supporting Variants
Samples
Known GenesC1orf127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051163
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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