A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257931



Internal ID21400254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145694013..145694386hg38UCSC Ensembl
chr4:146615165..146615538hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730167
Supporting Variants
SamplesNA19239
Known GenesC4orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257931
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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