A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017613



Internal ID19106830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:133155437..133168229hg38UCSC Ensembl
Innerchr8:134167681..134180473hg19UCSC Ensembl
Innerchr8:134236863..134249655hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3812793
hg1912793
hg1812793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7323n100
Supporting Variantsnssv3691589, nssv3691587, nssv3691590, nssv3691581, nssv3691585, nssv3691586, nssv3691583, nssv3691591, nssv3691584, nssv3691582, nssv3691578, nssv3691588, nssv3691579, nssv3691580, nssv3691577
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)nsv1017613
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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