A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536892



Internal ID20910236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99947638..99948529hg38UCSC Ensembl
chr1:100413194..100414085hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv279n223
Supporting Variantsnssv18252831
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536892
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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