A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582988



Internal ID18881269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159385913..159456887hg38UCSC Ensembl
Innerchr2:160242424..160313398hg19UCSC Ensembl
Innerchr2:159950670..160021644hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3870975
hg1970975
hg1870975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003926
Supporting Variants
Samples
Known GenesBAZ2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582988
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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