A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060652



Internal ID20627692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27253912..27256556hg38UCSC Ensembl
chr1:27580403..27583047hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325157
Supporting Variants
Samples
Known GenesWDTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060652
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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