A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028855



Internal ID19118074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62589040..63273371hg38UCSC Ensembl
Innerchr7:62049418..62733749hg19UCSC Ensembl
Innerchr7:61686853..62371184hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38684332
hg19684332
hg18684332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6411n100
Supporting Variantsnssv3753024
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028855
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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