A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060657



Internal ID20627697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27371956..27377130hg38UCSC Ensembl
chr1:27698447..27703622hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385175
hg195176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323537
Supporting Variants
Samples
Known GenesFCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060657
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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