A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256607



Internal ID21398668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218929..6220353hg38UCSC Ensembl
chrX:6136970..6138394hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730244
Supporting Variants
SamplesHG00514
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256607
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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