A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730047



Internal ID21400863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123974835..123997558hg38UCSC Ensembl
chr9:126737114..126759837hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3822724
hg1922724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257044, nssv16258237, nssv16256289, nssv16256898, nssv16258783, nssv16258726, nssv16258563, nssv16257041, nssv16258398, nssv16256113, nssv16256390, nssv16257345, nssv16258211, nssv16258224, nssv16258331, nssv16257569, nssv16257398, nssv16257157, nssv16257957, nssv16256471, nssv16258297, nssv16257004, nssv16256170, nssv16258108, nssv16257028, nssv16258100, nssv16255930, nssv16256920
SamplesNA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730047
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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