A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019911



Internal ID19109129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110865917..110930185hg38UCSC Ensembl
Innerchr7:110505973..110570241hg19UCSC Ensembl
Innerchr7:110293209..110357477hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3864269
hg1964269
hg1864269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751486, nssv3645218
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019911
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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