A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579463



Internal ID20952534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73075995..73076171hg38UCSC Ensembl
chr10:74835753..74835929hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228887
Samples
Known GenesP4HA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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