A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547197



Internal ID20920402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44155626..44157235hg38UCSC Ensembl
chr1:44621298..44622907hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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