A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014442



Internal ID19103660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:202428356..202447466hg38UCSC Ensembl
Innerchr2:203293079..203312189hg19UCSC Ensembl
Innerchr2:203001324..203020434hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3819111
hg1919111
hg1819111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4150n100
Supporting Variantsnssv3584029, nssv3584030, nssv3584032, nssv3584031, nssv3584028
Samples
Known GenesBMPR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014442
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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