A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6620n100



Internal ID22792707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131360548..131424837hg38UCSC Ensembl
chr7:131045307..131109596hg19UCSC Ensembl
chr7:130695847..130760136hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3864290
hg1964290
hg1864290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033636, nsv1020375, nsv1028722
Samples
Known GenesMKLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6620n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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