A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6621n100



Internal ID22792708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131369169..131462692hg38UCSC Ensembl
chr7:131053928..131147451hg19UCSC Ensembl
chr7:130704468..130797991hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3893524
hg1993524
hg1893524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019529, nsv1025938, nsv1033250
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)dgv6621n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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