A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127688



Internal ID18913190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:45004346..45004415hg38UCSC Ensembl
Outerchr19:45507604..45507673hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956220
SamplesKWS1
Known GenesRELB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127688
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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