A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029300



Internal ID18771832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2997310..3024828hg38UCSC Ensembl
Innerchr6:2997544..3025062hg19UCSC Ensembl
Innerchr6:2942543..2970061hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3827519
hg1927519
hg1827519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654722
Samples
Known GenesHTATSF1P2, NQO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029300
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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