A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3661226



Internal ID18612821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:43029785..43072177hg38UCSC Ensembl
Innerchr7:43069384..43111776hg19UCSC Ensembl
Innerchr7:43035909..43078301hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3842393
hg1942393
hg1842393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035016
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)nssv3661226
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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