A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134066



Internal ID19269194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:123764437..123764496hg38UCSC Ensembl
Outerchr10:125523953..125524012hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985506, nssv3970405
SamplesKWS2, KWS1
Known GenesCPXM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134066
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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