A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003296



Internal ID19189999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9225092..9225462hg38UCSC Ensembl
Outerchr18:9225090..9225460hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154023
Supporting Variants
SamplesKWB1
Known GenesANKRD12
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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