A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030538



Internal ID19119757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91716524..91729627hg38UCSC Ensembl
Innerchr7:91345839..91358942hg19UCSC Ensembl
Innerchr7:91183775..91196878hg18UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3813104
hg1913104
hg1813104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655245
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)nsv1030538
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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