A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334230



Internal ID20867413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171056840..171176302hg38UCSC Ensembl
chr1:171025981..171145441hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38119463
hg19119461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053998
Samples
Known GenesFMO3, FMO6P, MIR1295A, MIR1295B, MROH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334230
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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