A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019049



Internal ID19108266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:98037511..98106878hg38UCSC Ensembl
Innerchr5:97373215..97442582hg19UCSC Ensembl
Innerchr5:97398971..97468338hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3869368
hg1969368
hg1869368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640467
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)nsv1019049
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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