A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595131



Internal ID20968202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62037381..62039767hg38UCSC Ensembl
chr17:60114742..60117128hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382387
hg192387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242542
Samples
Known GenesMED13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595131
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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