A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559714



Internal ID20932785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99058374..99059131hg38UCSC Ensembl
chr7:98655997..98656754hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275834
Samples
Known GenesSMURF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559714
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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