A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033776



Internal ID19122997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143921485..144022444hg38UCSC Ensembl
Innerchr4:144842638..144943597hg19UCSC Ensembl
Innerchr4:145062088..145163047hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38100960
hg19100960
hg18100960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5423n100
Supporting Variantsnssv3635232, nssv3635233
Samples
Known GenesGYPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033776
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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