A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022680



Internal ID18765214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35906411..35969946hg38UCSC Ensembl
Innerchr7:35946021..36009556hg19UCSC Ensembl
Innerchr7:35912546..35976081hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3863536
hg1963536
hg1863536
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6321n100
Supporting Variantsnssv3643417, nssv3643423, nssv3643414, nssv3643421, nssv3643413, nssv3643418, nssv3643415, nssv3643419, nssv3643420, nssv3643416, nssv3643422
Samples
Known GenesSEPT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022680
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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