A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026718



Internal ID18769249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7896694..7969833hg38UCSC Ensembl
Innerchr8:7754216..7827355hg19UCSC Ensembl
Innerchr8:7791626..7864765hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3873140
hg1973140
hg1873140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6972n100
Supporting Variantsnssv3681182, nssv3681181, nssv3681180
Samples
Known GenesDEFB4A, FAM66E, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026718
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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