A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019516



Internal ID19108734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:129833664..130055047hg38UCSC Ensembl
Innerchr4:130754819..130976202hg19UCSC Ensembl
Innerchr4:130974269..131195652hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg38221384
hg19221384
hg18221384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743097
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)nsv1019516
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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