A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009685



Internal ID19098903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96387150..96470905hg38UCSC Ensembl
Innerchr4:97308301..97392056hg19UCSC Ensembl
Innerchr4:97527324..97611079hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3883756
hg1983756
hg1883756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5343n100
Supporting Variantsnssv3630987
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)nsv1009685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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