A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033542



Internal ID19122763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91745013..91767109hg38UCSC Ensembl
Innerchr7:91374328..91396424hg19UCSC Ensembl
Innerchr7:91212264..91234360hg18UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3822097
hg1922097
hg1822097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655247
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)nsv1033542
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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