A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556496



Internal ID20929567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75545481..75548222hg38UCSC Ensembl
chr7:75174779..75177520hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382742
hg192742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276547
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556496
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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