A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054604



Internal ID19143823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43003719..43036583hg38UCSC Ensembl
Innerchr10:43499167..43532031hg19UCSC Ensembl
Innerchr10:42819173..42852037hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3832865
hg1932865
hg1832865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522711
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)nsv1054604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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