A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6347n100



Internal ID20157963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50603653..50626760hg38UCSC Ensembl
chr7:50671350..50694457hg19UCSC Ensembl
chr7:50638844..50661951hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3823108
hg1923108
hg1823108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021753, nsv1020791
Samples
Known GenesGRB10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6347n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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