A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037949



Internal ID19127168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56541038..56595165hg38UCSC Ensembl
Innerchr10:58300798..58354925hg19UCSC Ensembl
Innerchr10:57970804..58024931hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3854128
hg1954128
hg1854128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504448
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)nsv1037949
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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