A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14269271



Internal ID22291654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:1401507..1437299hg38UCSC Ensembl
OuterchrX:1520400..1556192hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3835793
hg1935793
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207262
Supporting Variants
SamplesNA19240
Known GenesASMTL, ASMTL-AS1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14269271
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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