A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023653



Internal ID19112870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79691200..79780757hg38UCSC Ensembl
Innerchr7:79320516..79410073hg19UCSC Ensembl
Innerchr7:79158452..79248009hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3889558
hg1989558
hg1889558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6512n100
Supporting Variantsnssv3755410
Samples
Known GenesMIR548M
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023653
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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