A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004429



Internal ID19093647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109880874..110949984hg38UCSC Ensembl
Innerchr3:109599721..110668831hg19UCSC Ensembl
Innerchr3:111082411..112151521hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381069111
hg191069111
hg181069111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604408
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)nsv1004429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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