A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112824



Internal ID19274967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:44893808..44894508hg38UCSC Ensembl
Outerchr3:44935300..44936000hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2518n106
Supporting Variantsnssv3967322
SamplesKWS2
Known GenesTGM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112824
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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