A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995922



Internal ID15582106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:127813308..127964256hg38UCSC Ensembl
Innerchr5:127149000..127299948hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38150949
hg19150949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483040
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995922
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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