A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580055



Internal ID20953126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74676533..74677231hg38UCSC Ensembl
chr10:76436291..76436989hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219758
Samples
Known GenesADK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580055
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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