A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015974



Internal ID19105192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109770248..109813913hg38UCSC Ensembl
Innerchr7:109410305..109453970hg19UCSC Ensembl
Innerchr7:109197541..109241206hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3843666
hg1943666
hg1843666
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6550n100
Supporting Variantsnssv3656244, nssv3656243
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)nsv1015974
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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