A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134979



Internal ID19273964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:35304350..35304614hg38UCSC Ensembl
Outerchr10:35593278..35593542hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv396n106
Supporting Variantsnssv3988519
SamplesKWS2
Known GenesCCNY
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134979
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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