A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033664



Internal ID19122885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25432262..25463772hg38UCSC Ensembl
Innerchr7:25471881..25503391hg19UCSC Ensembl
Innerchr7:25438406..25469916hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3831511
hg1931511
hg1831511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6308n100
Supporting Variantsnssv3643307
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)nsv1033664
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer