A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573595



Internal ID20946666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39459968..39461691hg38UCSC Ensembl
chr4:39461588..39463311hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265150
Samples
Known GenesLIAS, MIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573595
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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