A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022986



Internal ID19112203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7169132..7189812hg38UCSC Ensembl
Innerchr5:7169245..7189925hg19UCSC Ensembl
Innerchr5:7222245..7242925hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3820681
hg1920681
hg1820681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5560n100
Supporting Variantsnssv3638607, nssv3638608
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)nsv1022986
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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