A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582549



Internal ID20955620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73219483..73220486hg38UCSC Ensembl
chr17:71215622..71216625hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244571
Samples
Known GenesFAM104A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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