A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317734



Internal ID20850822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:172659707..172664451hg38UCSC Ensembl
chr1:172628847..172633591hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg384745
hg194745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053930
Samples
Known GenesFASLG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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