A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14271176



Internal ID22282767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9795815..9817089hg38UCSC Ensembl
OuterchrY:9633424..9654698hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3821275
hg1921275
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192239
Supporting Variants
SamplesNA19239
Known GenesTTTY22
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14271176
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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