A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247261



Internal ID21302736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108733582..108955957hg38UCSC Ensembl
Outerchr7:108727361..108966081hg38UCSC Ensembl
Innerchr7:108374026..108596014hg19UCSC Ensembl
Outerchr7:108367805..108606138hg19UCSC Ensembl
Innerchr7:108161262..108383250hg18UCSC Ensembl
Outerchr7:108155041..108393374hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38238721
hg19238334
hg18238334
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170056
Supporting Variants
SamplesMLY_17
Known GenesC7orf66
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247261
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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