A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030971



Internal ID19120192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136669376..136851683hg38UCSC Ensembl
Innerchr8:137681619..137863926hg19UCSC Ensembl
Innerchr8:137750801..137933108hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38182308
hg19182308
hg18182308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3689996, nssv3689992, nssv3689987, nssv3689994, nssv3689990, nssv3689993, nssv3689991, nssv3689995, nssv3689989, nssv3689988
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)nsv1030971
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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