A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551530



Internal ID20924664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44712960..44714268hg38UCSC Ensembl
chr1:45178632..45179940hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251851
Samples
Known GenesC1orf228
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551530
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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