A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586916



Internal ID18538511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:234032646..234055672hg38UCSC Ensembl
Innerchr2:234941290..234964316hg19UCSC Ensembl
Innerchr2:234606029..234629055hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3823027
hg1923027
hg1823027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007335
Supporting Variants
Samples
Known GenesSPP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586916
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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