A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029935



Internal ID19119154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130820615..130936382hg38UCSC Ensembl
Innerchr4:131741770..131857537hg19UCSC Ensembl
Innerchr4:131961220..132076987hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38115768
hg19115768
hg18115768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639454
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)nsv1029935
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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