A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561576



Internal ID20934647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39914957..39916326hg38UCSC Ensembl
chr7:39954556..39955925hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6655n223
Supporting Variantsnssv18275257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561576
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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