A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505287



Internal ID18803568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97103220..97173558hg38UCSC Ensembl
Innerchr11:96974220..97044558hg19UCSC Ensembl
Innerchr11:96479430..96549768hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3870339
hg1970339
hg1870339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037706
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)nssv3505287
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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