A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110911



Internal ID19277203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:107083255..107089155hg38UCSC Ensembl
Outerchr7:106723700..106729600hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3640n106
Supporting Variantsnssv3961327
SamplesKWS1
Known GenesPRKAR2B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110911
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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