A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143648



Internal ID18908555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112949441..112951941hg38UCSC Ensembl
Outerchr10:114709200..114711700hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382501
hg192501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv518n106
Supporting Variantsnssv3994335
SamplesKWS1
Known GenesTCF7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143648
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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