A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv972940



Internal ID15920210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127552477..127685471hg38UCSC Ensembl
Innerchr3:127271320..127404314hg19UCSC Ensembl
Innerchr3:128754010..128887004hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38132995
hg19132995
hg18132995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591581
Supporting Variants
Samples
Known GenesABTB1, MCM2, MIR6825, PODXL2, TPRA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv972940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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