A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005010



Internal ID18747541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:100386517..100409430hg38UCSC Ensembl
Innerchr4:101307674..101330587hg19UCSC Ensembl
Innerchr4:101526697..101549610hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3822914
hg1922914
hg1822914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3631008
Samples
Known GenesEMCN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005010
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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