A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018249



Internal ID19107466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136849867hg38UCSC Ensembl
Innerchr8:137681619..137862110hg19UCSC Ensembl
Innerchr8:137750801..137931292hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38180492
hg19180492
hg18180492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3692755, nssv3692752, nssv3692753, nssv3757392, nssv3692754
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)nsv1018249
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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