A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007884



Internal ID19097103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31070312..31679001hg38UCSC Ensembl
Innerchr4:31071934..31680623hg19UCSC Ensembl
Innerchr4:30681032..31289721hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38608690
hg19608690
hg18608690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620637
Samples
Known GenesPCDH7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007884
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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