A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258633



Internal ID21397970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52077148..52176853hg38UCSC Ensembl
chrX:51820244..51919949hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3899706
hg1999706
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730085
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258633
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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