A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589699



Internal ID20962770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30622400..30771324hg38UCSC Ensembl
chr17:28949418..29098342hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38148925
hg19148925
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241775
Samples
Known GenesLRRC37BP1, SH3GL1P2, SUZ12P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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