A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029148



Internal ID15535648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42628506..42630173hg38UCSC Ensembl
Innerchr5:42628608..42630275hg19UCSC Ensembl
Innerchr5:42664365..42666032hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381668
hg191668
hg181668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597890
Supporting Variants
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1029148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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