A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323873



Internal ID20856996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154189695..154207176hg38UCSC Ensembl
chr1:154162171..154179652hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3817482
hg1917482
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200502
Samples
Known GenesC1orf189, C1orf43, MIR190B, TPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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