A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573948



Internal ID20947019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2839372..2839764hg38UCSC Ensembl
chr7:2879006..2879398hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273426
Samples
Known GenesGNA12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573948
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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