A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598603



Internal ID20971674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4262367..4610905hg38UCSC Ensembl
chr19:4262364..4610917hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38348539
hg19348554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246316
Samples
Known GenesCCDC94, CHAF1A, FSD1, HDGFRP2, LRG1, MIR4746, MPND, PLIN4, PLIN5, SEMA6B, SH3GL1, SHD, STAP2, TMIGD2, UBXN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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