A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017226



Internal ID19106443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85934047..86130557hg38UCSC Ensembl
Innerchr7:85563363..85759873hg19UCSC Ensembl
Innerchr7:85401299..85597809hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38196511
hg19196511
hg18196511
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6522n100
Supporting Variantsnssv3655182
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)nsv1017226
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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