A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115931



Internal ID19283292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10135691..10203491hg38UCSC Ensembl
OuterchrY:9973300..10041100hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3867801
hg1967801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4342n106
Supporting Variantsnssv3978493
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115931
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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