A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034655



Internal ID19123876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136848746hg38UCSC Ensembl
Innerchr8:137681619..137860989hg19UCSC Ensembl
Innerchr8:137750801..137930171hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38179371
hg19179371
hg18179371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692751
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)nsv1034655
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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