A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029748



Internal ID18772279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:7271371..7310026hg38UCSC Ensembl
Innerchr6:7271604..7310259hg19UCSC Ensembl
Innerchr6:7216603..7255258hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3838656
hg1938656
hg1838656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654746
Samples
Known GenesSSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029748
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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