A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023949



Internal ID19113166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155132067..155165289hg38UCSC Ensembl
Innerchr7:154923777..154956999hg19UCSC Ensembl
Innerchr7:154554710..154587932hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3833223
hg1933223
hg1833223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674668
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)nsv1023949
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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