A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017279



Internal ID19106496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:29618843..29731279hg38UCSC Ensembl
Innerchr7:29658459..29770895hg19UCSC Ensembl
Innerchr7:29624984..29737420hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38112437
hg19112437
hg18112437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6313n100
Supporting Variantsnssv3643334
Samples
Known GenesDPY19L2P3, LOC646762, MIR550A3, ZNRF2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017279
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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