A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022764



Internal ID18765298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:78281755..78687291hg38UCSC Ensembl
Innerchr7:77911072..78316607hg19UCSC Ensembl
Innerchr7:77749008..78154543hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38405537
hg19405536
hg18405536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657117
Samples
Known GenesMAGI2, MIR548AU, RPL13AP17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022764
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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