A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029358



Internal ID15535858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42630071..42630866hg38UCSC Ensembl
Innerchr5:42630173..42630968hg19UCSC Ensembl
Innerchr5:42665930..42666725hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38796
hg19796
hg18796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597919
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)nssv1029358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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