A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583257



Internal ID20956328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30685265..30896219hg38UCSC Ensembl
chr17:29012283..29223237hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38210955
hg19210955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241781
Samples
Known GenesATAD5, CRLF3, SUZ12P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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