A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320889



Internal ID20853990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51125054..51134919hg38UCSC Ensembl
chr1:51590726..51600591hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg389866
hg199866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201440
Samples
Known GenesC1orf185
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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