A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577256



Internal ID20950327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44772858..44808462hg38UCSC Ensembl
chr17:42850226..42885830hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3835605
hg1935605
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242341
Samples
Known GenesADAM11, GJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577256
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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