A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318130



Internal ID20851221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227560402..227562285hg38UCSC Ensembl
chr1:227748103..227749986hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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