A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017797



Internal ID19107014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55494191..55540031hg38UCSC Ensembl
Innerchr7:55561884..55607724hg19UCSC Ensembl
Innerchr7:55529378..55575218hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3845841
hg1945841
hg1845841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661412
Samples
Known GenesVOPP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017797
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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