A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019490



Internal ID18762025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:125927450..126221150hg38UCSC Ensembl
Innerchr6:126248596..126542296hg19UCSC Ensembl
Innerchr6:126290289..126583989hg18UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38293701
hg19293701
hg18293701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654380
Samples
Known GenesHINT3, MIR5695, NCOA7, TRMT11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019490
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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