A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177703



Internal ID22334569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52700209..52787377hg38UCSC Ensembl
chrX:52729259..52816422hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3887169
hg1987164
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439959, nssv14439958
SamplesHG00733
Known GenesSSX2, SSX2B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177703
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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