A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570285



Internal ID20943356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7795440..7796714hg38UCSC Ensembl
chr4:7797167..7798441hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381275
hg191275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5146n223
Supporting Variantsnssv18265315
Samples
Known GenesAFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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