A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563936



Internal ID20937007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114202066..114203056hg38UCSC Ensembl
chr7:113842121..113843111hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38991
hg19991
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7091n223
Supporting Variantsnssv18273711
Samples
Known GenesFOXP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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