A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004353



Internal ID19093570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49559956..49656583hg38UCSC Ensembl
Innerchr4:49561973..49658600hg19UCSC Ensembl
Innerchr4:49256730..49353357hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3896628
hg1996628
hg1896628
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625250, nssv3625249
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)nsv1004353
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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