A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025407



Internal ID19114625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171626934..171700659hg38UCSC Ensembl
Innerchr4:172548085..172621810hg19UCSC Ensembl
Innerchr4:172784660..172858385hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3873726
hg1973726
hg1873726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635434
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025407
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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