A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177359



Internal ID22334383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12744294..12744383hg38UCSC Ensembl
chrX:12762413..12762502hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10036n152
Supporting Variantsnssv14439699
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177359
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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