A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643138



Internal ID18941419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13577990..13696321hg38UCSC Ensembl
Innerchr7:13617615..13735946hg19UCSC Ensembl
Innerchr7:13584140..13702471hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38118332
hg19118332
hg18118332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023839
Supporting Variants
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)nssv3643138
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