A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019418



Internal ID19108636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19158481..19185179hg38UCSC Ensembl
Innerchr7:19198104..19224802hg19UCSC Ensembl
Innerchr7:19164629..19191327hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3826699
hg1926699
hg1826699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6300n100
Supporting Variantsnssv3752920, nssv3643242
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)nsv1019418
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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