A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963510



Internal ID19219089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:11512052..11549368hg38UCSC Ensembl
OuterchrY:13667728..13705044hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3837317
hg1937317
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111395
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963510
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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