A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994335



Internal ID18868459
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 StatusS
Merged Variantsnsv1143648
Supporting Variants
SamplesKWS1
Known GenesTCF7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994335
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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