A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573695



Internal ID20946766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17344633..17345327hg38UCSC Ensembl
chr7:17384257..17384951hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273836
Samples
Known GenesAHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573695
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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