A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567707



Internal ID20940778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70659353..70660488hg38UCSC Ensembl
chr4:71525070..71526205hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265949
Samples
Known GenesIGJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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