A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002953



Internal ID18745485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142177810..142208338hg38UCSC Ensembl
Innerchr3:141896652..141927180hg19UCSC Ensembl
Innerchr3:143379342..143409870hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3830529
hg1930529
hg1830529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606121
Samples
Known GenesGK5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002953
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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