A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173111



Internal ID22332158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140722716..140725526hg38UCSC Ensembl
chrX:139804881..139807691hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14438688, nssv14438687, nssv14413713, nssv14413712
SamplesHG00733, HG00514
Known GenesLINC00632
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173111
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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