A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2857797



Internal ID15726750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210431713..210438609hg38UCSC Ensembl
Innerchr1:210605057..210611953hg19UCSC Ensembl
Innerchr1:208671680..208678576hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg386897
hg196897
hg186897
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514040
Supporting Variants
SamplesNA19095
Known GenesHHAT
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2857797
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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