A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138606



Internal ID19272595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9205264..9205323hg38UCSC Ensembl
Outerchr18:9205262..9205321hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991195
SamplesKWS2
Known GenesANKRD12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138606
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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