A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135110



Internal ID18914210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:226152847..226153091hg38UCSC Ensembl
Outerchr2:227017563..227017807hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2161n106
Supporting Variantsnssv3988662
SamplesKWS2
Known GenesLOC646736
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135110
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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