A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751487



Internal ID19049768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111131505..111178402hg38UCSC Ensembl
Innerchr7:110771561..110818458hg19UCSC Ensembl
Innerchr7:110558797..110605694hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3846898
hg1946898
hg1846898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029168
Supporting Variants
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)nssv3751487
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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