A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149465



Internal ID19199664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14222606..14222777hg38UCSC Ensembl
Outerchr18:14222605..14222776hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000761
SamplesKWB1
Known GenesANKRD20A5P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149465
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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