A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031419



Internal ID19120641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118068680..118099346hg38UCSC Ensembl
Innerchr7:117708734..117739400hg19UCSC Ensembl
Innerchr7:117495970..117526636hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3830667
hg1930667
hg1830667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6594n100
Supporting Variantsnssv3662054
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)nsv1031419
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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