A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028020



Internal ID19117238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79177910..79223365hg38UCSC Ensembl
Innerchr7:78807226..78852681hg19UCSC Ensembl
Innerchr7:78645162..78690617hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3845456
hg1945456
hg1845456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6511n100
Supporting Variantsnssv3657171, nssv3657170, nssv3657174, nssv3657173, nssv3657172, nssv3657175
Samples
Known GenesMAGI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028020
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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