A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007556



Internal ID19096775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..35885hg38UCSC Ensembl
Innerchr4:12269..35885hg19UCSC Ensembl
Innerchr4:2269..25885hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3823617
hg1923617
hg1823617
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5050n100
Supporting Variantsnssv3617047, nssv3617052, nssv3617050, nssv3617049, nssv3737885, nssv3617051, nssv3617048
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)nsv1007556
Frequency
Sample Size11257
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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