A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003926



Internal ID19093144
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 StatusM
Merged Variants
Supporting Variantsnssv3582988
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)nsv1003926
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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