A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023464



Internal ID18765997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35900957..35962451hg38UCSC Ensembl
Innerchr7:35940567..36002061hg19UCSC Ensembl
Innerchr7:35907092..35968586hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3861495
hg1961495
hg1861495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6321n100
Supporting Variantsnssv3643412
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)nsv1023464
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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