A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243155



Internal ID20810195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61696749..61697882hg38UCSC Ensembl
chr17:59774110..59775243hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381134
hg191134
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591767
Supporting Variants
Samples
Known GenesBRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243155
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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