A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115919



Internal ID19260948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:1198443..1363007hg38UCSC Ensembl
OuterchrY:1267300..1431900hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38164565
hg19164601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978481
SamplesKWS2
Known GenesCRLF2, CSF2RA, IL3RA, MIR3690, MIR3690-2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115919
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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