A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013341



Internal ID19102559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92667572..92771936hg38UCSC Ensembl
Innerchr4:93588723..93693087hg19UCSC Ensembl
Innerchr4:93807746..93912110hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38104365
hg19104365
hg18104365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630970
Samples
Known GenesGRID2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013341
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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