A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145302



Internal ID19256795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:18216614..18237614hg38UCSC Ensembl
OuterchrY:20378500..20399500hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3821001
hg1921001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982391
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145302
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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