A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961799



Internal ID19224950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24246053..24263853hg38UCSC Ensembl
OuterchrY:26392200..26410000hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3817801
hg1917801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129123
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961799
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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