A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996561



Internal ID15582062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:112870506..113009256hg38UCSC Ensembl
Innerchr7:112510561..112649311hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38138751
hg19138751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483110
Supporting Variants
Samples
Known GenesC7orf60
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996561
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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