A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730187



Internal ID21400998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61785368..62487139hg38UCSC Ensembl
chr9:44958294..46798440hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38701772
hg191840147
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258290, nssv16258500, nssv16257305, nssv16255947, nssv16257025, nssv16257716, nssv16258105, nssv16258557, nssv16255982, nssv16256547, nssv16257515, nssv16258057, nssv16258509, nssv16255877, nssv16257200, nssv16256310, nssv16257438
SamplesNA19238, NA19239, NA19240, HG00513
Known GenesFAM27A, FAM27C, FAM27E1, FAM27E2, KGFLP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730187
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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