A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959387



Internal ID19208858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:56829352..56829447hg38UCSC Ensembl
OuterchrY:58975499..58975594hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110122
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959387
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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