A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555141



Internal ID20928230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42772608..42774073hg38UCSC Ensembl
chr1:43238279..43239744hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381466
hg191466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv169n223
Supporting Variantsnssv18250984
Samples
Known GenesC1orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555141
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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