A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010290



Internal ID19099507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92831984..92908850hg38UCSC Ensembl
Innerchr4:93753135..93830001hg19UCSC Ensembl
Innerchr4:93972158..94049024hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3876867
hg1976867
hg1876867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3742893
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)nsv1010290
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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