A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011636



Internal ID19100853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:33999447..35826250hg38UCSC Ensembl
Innerchr4:34001069..35827872hg19UCSC Ensembl
Innerchr4:33677464..35504267hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381826804
hg191826804
hg181826804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620653
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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