A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998669



Internal ID18811519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63850701..64580449hg38UCSC Ensembl
Innerchr4:64716419..65446167hg19UCSC Ensembl
Innerchr4:64399014..65128762hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38729749
hg19729749
hg18729749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3740171
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)nsv998669
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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