A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996097



Internal ID19189188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:25924552..25936853hg38UCSC Ensembl
OuterchrY:28070699..28083000hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3812302
hg1912302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150623
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996097
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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