A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978489



Internal ID19235932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9860691..9876391hg38UCSC Ensembl
OuterchrY:9698300..9714000hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3815701
hg1915701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115927
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978489
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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