A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012062



Internal ID18754598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64277750..64318606hg38UCSC Ensembl
Innerchr4:65143468..65184324hg19UCSC Ensembl
Innerchr4:64826063..64866919hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3840857
hg1940857
hg1840857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625949
Samples
Known GenesTECRL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012062
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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