A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000398



Internal ID17293350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:20260315..20329314hg38UCSC Ensembl
OuterchrY:22422201..22491200hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3869000
hg1969000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953110
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000398
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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