A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710120



Internal ID19008401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48064599..48104179hg38UCSC Ensembl
Innerchr11:48086151..48125731hg19UCSC Ensembl
Innerchr11:48042727..48082307hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3839581
hg1939581
hg1839581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053528
Supporting Variants
Samples
Known GenesPTPRJ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710120
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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