A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256731



Internal ID21399987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154341329..154390400hg38UCSC Ensembl
chrX:153569679..153618760hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3849072
hg1949082
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730161
Supporting Variants
SamplesNA19238
Known GenesEMD, FLNA
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256731
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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