A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006642



Internal ID19095859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7785253..7809564hg38UCSC Ensembl
Innerchr4:7786980..7811291hg19UCSC Ensembl
Innerchr4:7837880..7862191hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3824312
hg1924312
hg1824312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616187
Samples
Known GenesAFAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006642
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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