A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3630987



Internal ID18929268
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 StatusS
Merged Variantsnsv1009685
Supporting Variants
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)nssv3630987
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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