A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253084



Internal ID20820124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39781913..39782464hg38UCSC Ensembl
chr1:40247585..40248136hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542195
Supporting Variants
Samples
Known GenesBMP8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253084
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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