A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028108



Internal ID19117326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15265119..15334474hg38UCSC Ensembl
Innerchr7:15304744..15374099hg19UCSC Ensembl
Innerchr7:15271269..15340624hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3869356
hg1969356
hg1869356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752904
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028108
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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