A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587072



Internal ID20960143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44422690..44423210hg38UCSC Ensembl
chr17:42500058..42500578hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242307
Samples
Known GenesGPATCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587072
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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