A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023992



Internal ID19113209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20014193..20065052hg38UCSC Ensembl
Innerchr7:20053816..20104675hg19UCSC Ensembl
Innerchr7:20020341..20071200hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3850860
hg1950860
hg1850860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643265, nssv3643264
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)nsv1023992
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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