A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556681



Internal ID20929752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75068151..75069163hg38UCSC Ensembl
chr7:74483964..74484977hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381013
hg191014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276542
Samples
Known GenesWBSCR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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