A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575122



Internal ID20948193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:149368566..149369014hg38UCSC Ensembl
chr4:150289718..150290166hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5514n223
Supporting Variantsnssv18263768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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