A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140104



Internal ID19282110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24170453..24194553hg38UCSC Ensembl
OuterchrY:26316600..26340700hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3824101
hg1924101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978815
SamplesKWS2
Known GenesCSPG4P1Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140104
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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