A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536776



Internal ID20910119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61498754..61514285hg38UCSC Ensembl
chr1:61964426..61979957hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815532
hg1915532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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