A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150778



Internal ID19198545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:74514499..74514570hg38UCSC Ensembl
Outerchr18:72181734..72181805hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996247
SamplesKWB1
Known GenesCNDP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150778
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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