A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033855



Internal ID19123076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4823046..5030133hg38UCSC Ensembl
Innerchr7:4862677..5069764hg19UCSC Ensembl
Innerchr7:4829203..5036290hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38207088
hg19207088
hg18207088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6238n100
Supporting Variantsnssv3655051
Samples
Known GenesMMD2, PAPOLB, RADIL, RNF216P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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