A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577440



Internal ID20950511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36507873..36562212hg38UCSC Ensembl
chr17:34863712..34918052hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3854340
hg1954341
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242190
Samples
Known GenesGGNBP2, MYO19, PIGW
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577440
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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