A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102246



Internal ID21276261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21378030..21382658hg38UCSC Ensembl
InnerchrY:23539916..23544544hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg384629
hg194629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116096
Supporting Variants
Samplessample234
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102246
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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