A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730050



Internal ID21400866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34540845..34562456hg38UCSC Ensembl
chr14:35010051..35031662hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3821612
hg1921612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258843, nssv16256970, nssv16258459, nssv16258809, nssv16256768, nssv16258229, nssv16257954, nssv16258575, nssv16256631, nssv16256129, nssv16258104, nssv16257794, nssv16258250, nssv16256691, nssv16255912, nssv16258467
SamplesNA19238, HG00731, HG00732, HG00733
Known GenesSNX6
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730050
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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