A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585333



Internal ID20958404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74996232..74997170hg38UCSC Ensembl
chr17:72992327..72993265hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3247n223
Supporting Variantsnssv18244594
Samples
Known GenesCDR2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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