A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112728



Internal ID18938457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:344100..344900hg38UCSC Ensembl
Outerchr19:344100..344900hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1667n106
Supporting Variantsnssv3967221
SamplesKWS2
Known GenesMIER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112728
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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