A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751490



Internal ID19049771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111194962..111626076hg38UCSC Ensembl
Innerchr7:110835018..111266132hg19UCSC Ensembl
Innerchr7:110622254..111053368hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38431115
hg19431115
hg18431115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019130
Supporting Variants
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)nssv3751490
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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