A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996374



Internal ID15581875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101960725..102138706hg38UCSC Ensembl
Innerchr7:101604005..101781986hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38177982
hg19177982
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483094
Supporting Variants
Samples
Known GenesCUX1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996374
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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