A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030222



Internal ID19119441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108169482..108204472hg38UCSC Ensembl
Innerchr7:107809927..107844916hg19UCSC Ensembl
Innerchr7:107597163..107632152hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3834991
hg1934990
hg1834990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755480
Samples
Known GenesNRCAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030222
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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