A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764003



Internal ID19308185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77184145..77185329hg38UCSC Ensembl
chr18:74896101..74897285hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072818
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764003
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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