A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030758



Internal ID19119977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62720720..63246026hg38UCSC Ensembl
Innerchr7:62181098..62706404hg19UCSC Ensembl
Innerchr7:61818533..62343839hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38525307
hg19525307
hg18525307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6429n100
Supporting Variantsnssv3753032, nssv3753033
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)nsv1030758
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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