A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764971



Internal ID18967297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10462421..10462635hg38UCSC Ensembl
chr18:10462418..10462632hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071830
Supporting Variants
SamplesKWP1
Known GenesAPCDD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764971
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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