A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128832



Internal ID19264545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:70286464..70289664hg38UCSC Ensembl
Outerchr18:67953700..67956900hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg383201
hg193201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961500
SamplesKWS1
Known GenesSOCS6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128832
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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