A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568765



Internal ID20941836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3143156..3143901hg38UCSC Ensembl
chr4:3144883..3145628hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265089
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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