A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115945



Internal ID19270564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26285953..26299153hg38UCSC Ensembl
OuterchrY:28432100..28445300hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3813201
hg1913201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978508
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115945
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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