A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026868



Internal ID18769399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72532208..72859219hg38UCSC Ensembl
Innerchr7:71997193..72329779hg19UCSC Ensembl
Innerchr7:71635129..71967715hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38327012
hg19332587
hg18332587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6460n100
Supporting Variantsnssv3655716, nssv3655715
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026868
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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