A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010832



Internal ID19100049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569882..68620249hg38UCSC Ensembl
Innerchr4:69435600..69485967hg19UCSC Ensembl
Innerchr4:69118195..69168562hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3850368
hg1950368
hg1850368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5286n100
Supporting Variantsnssv3628903
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)nsv1010832
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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