A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017145



Internal ID18759680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127355250..127375405hg38UCSC Ensembl
Innerchr7:126995304..127015459hg19UCSC Ensembl
Innerchr7:126782540..126802695hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3820156
hg1920156
hg1820156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662179
Samples
Known GenesZNF800
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017145
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