A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140095



Internal ID19257635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10246291..10255291hg38UCSC Ensembl
OuterchrY:10083900..10092900hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg389001
hg199001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4344n106
Supporting Variantsnssv3978806
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140095
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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