A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29988



Internal ID12608182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16882837..16925672hg38UCSC Ensembl
Innerchr1:17209332..17252167hg19UCSC Ensembl
Innerchr1:17081919..17124754hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842836
hg1942836
hg1842836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84227
SamplesHuRef
Known GenesCROCC
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv29988
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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