A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150349



Internal ID19199477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24275952..24294453hg38UCSC Ensembl
OuterchrY:26422099..26440600hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3818502
hg1918502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003650
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150349
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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