A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149548



Internal ID19202160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:17507519..17519320hg38UCSC Ensembl
OuterchrY:19619399..19631200hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3811802
hg1911802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000852
SamplesKWB1
Known GenesFAM41AY1, FAM41AY2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149548
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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