A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007685



Internal ID19096904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:78811314..78867614hg38UCSC Ensembl
Innerchr4:79732468..79788768hg19UCSC Ensembl
Innerchr4:79951492..80007792hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3856301
hg1956301
hg1856301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5329n100
Supporting Variantsnssv3633883
Samples
Known GenesBMP2K
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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