A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025441



Internal ID19114659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:83117248..83178823hg38UCSC Ensembl
Innerchr5:82413067..82474642hg19UCSC Ensembl
Innerchr5:82448823..82510398hg18UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg3861576
hg1961576
hg1861576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639146
Samples
Known GenesXRCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025441
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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