A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527571



Internal ID15454864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:146299529..146312682hg38UCSC Ensembl
Innerchr6:146620665..146633818hg19UCSC Ensembl
Innerchr6:146662358..146675511hg18UCSC Ensembl
Innerchr6:146662358..146675511hg17UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3813154
hg1913154
hg1813154
hg1713154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704032
Samples
Known GenesGRM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527571
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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