A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133897



Internal ID19251776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:121742141..121742197hg38UCSC Ensembl
Outerchr1:121483939..121483995hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv161n106
Supporting Variantsnssv3970219
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133897
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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