A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034347



Internal ID19123569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97727257..97905746hg38UCSC Ensembl
Innerchr5:97062961..97241450hg19UCSC Ensembl
Innerchr5:97088717..97267206hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38178490
hg19178490
hg18178490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5718n100
Supporting Variantsnssv3640461
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)nsv1034347
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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