A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577071



Internal ID20950142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35638507..35640208hg38UCSC Ensembl
chr17:33965526..33967227hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3089n223
Supporting Variantsnssv18242159
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577071
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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