A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128048



Internal ID19258810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:33845241..33845310hg38UCSC Ensembl
Outerchr4:33846863..33846932hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2765n106
Supporting Variantsnssv3957474
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128048
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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