A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132816



Internal ID19251798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26638053..26672953hg38UCSC Ensembl
OuterchrY:28784200..28819100hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3834901
hg1934901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4367n106
Supporting Variantsnssv3987608
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132816
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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