A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020731



Internal ID18763265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185591279..185802877hg38UCSC Ensembl
Innerchr4:186512433..186724031hg19UCSC Ensembl
Innerchr4:186749427..186961025hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38211599
hg19211599
hg18211599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744533
Samples
Known GenesSORBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020731
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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