A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111867



Internal ID19266264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35304278..35304608hg38UCSC Ensembl
Outerchr10:35593206..35593536hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv396n106
Supporting Variantsnssv3964779
SamplesKWS2
Known GenesCCNY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111867
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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