A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257669



Internal ID20824709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60870306..60870751hg38UCSC Ensembl
chr2:61097441..61097886hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38446
hg19446
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536000
Supporting Variants
Samples
Known GenesFLJ16341
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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