A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032721



Internal ID19121943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155178759..155197793hg38UCSC Ensembl
Innerchr7:154970469..154989503hg19UCSC Ensembl
Innerchr7:154601402..154620436hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3819035
hg1919035
hg1819035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6764n100
Supporting Variantsnssv3674679, nssv3674680
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)nsv1032721
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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