A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710717



Internal ID19008998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97380089..97602215hg38UCSC Ensembl
Innerchr11:97251089..97473215hg19UCSC Ensembl
Innerchr11:96756299..96978425hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38222127
hg19222127
hg18222127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043842
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710717
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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