A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317715



Internal ID20850803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155315784..155316172hg38UCSC Ensembl
chr1:155285575..155285963hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052068
Samples
Known GenesFDPS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317715
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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