A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568527



Internal ID20941598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149482584..149483520hg38UCSC Ensembl
chr7:149179675..149180611hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38937
hg19937
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7170n223
Supporting Variantsnssv18275236
Samples
Known GenesZNF746
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568527
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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