A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557924



Internal ID20930995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67574818..67576057hg38UCSC Ensembl
chr7:67039805..67041044hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557924
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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