A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562579



Internal ID20935650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49727436..50028542hg38UCSC Ensembl
chr7:49767032..50068138hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38301107
hg19301107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274546
Samples
Known GenesVWC2, ZPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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