A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023651



Internal ID19112868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:108662604..108744736hg38UCSC Ensembl
Innerchr7:108303048..108385180hg19UCSC Ensembl
Innerchr7:108090284..108172416hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3882133
hg1982133
hg1882133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656224
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)nsv1023651
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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