A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588805



Internal ID20961876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:74957707..75029417hg38UCSC Ensembl
chr17:72953802..73025512hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3871711
hg1971711
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244593
Samples
Known GenesCDR2L, HID1, ICT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588805
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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