A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054014



Internal ID20621054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177867628..177868283hg38UCSC Ensembl
chr1:177836763..177837418hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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