A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562298



Internal ID20935369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103130831..103131456hg38UCSC Ensembl
chr7:102771278..102771903hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271594
Samples
Known GenesNAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562298
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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