A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110641



Internal ID18935386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10134491..10217991hg38UCSC Ensembl
OuterchrY:9972100..10055600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3883501
hg1983501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4342n106
Supporting Variantsnssv3960296
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110641
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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