A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987602



Internal ID19211165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11179524..11349624hg38UCSC Ensembl
OuterchrY:13335200..13505300hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38170101
hg19170101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132810
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987602
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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