A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016827



Internal ID18759362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110661290..110706914hg38UCSC Ensembl
Innerchr7:110301346..110346970hg19UCSC Ensembl
Innerchr7:110088582..110134206hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845625
hg1945625
hg1845625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645217
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016827
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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