A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017700



Internal ID19106917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51974205..52004909hg38UCSC Ensembl
Innerchr8:52886765..52917469hg19UCSC Ensembl
Innerchr8:53049318..53080022hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3830705
hg1930705
hg1830705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3687502, nssv3687504, nssv3687501, nssv3687500, nssv3687506, nssv3687498, nssv3687503, nssv3687505, nssv3687499
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)nsv1017700
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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