A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008889



Internal ID19098107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92634401..92701470hg38UCSC Ensembl
Innerchr4:93555552..93622621hg19UCSC Ensembl
Innerchr4:93774575..93841644hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3867070
hg1967070
hg1867070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5339n100
Supporting Variantsnssv3630968
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)nsv1008889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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