A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117923



Internal ID19266087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18992640..18992716hg38UCSC Ensembl
OuterchrY:21154526..21154602hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980125
SamplesKWS2
Known GenesCD24, TTTY14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117923
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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