A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024532



Internal ID19113749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104640946..104659400hg38UCSC Ensembl
Innerchr7:104281393..104299847hg19UCSC Ensembl
Innerchr7:104068629..104087083hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3818455
hg1918455
hg1818455
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755475
Samples
Known GenesLHFPL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024532
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