A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571860



Internal ID20944931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70521147..70521647hg38UCSC Ensembl
chr4:71386864..71387364hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265942
Samples
Known GenesAMTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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