A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6618n100



Internal ID22792705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131332669..131381658hg38UCSC Ensembl
chr7:131017428..131066417hg19UCSC Ensembl
chr7:130667968..130716957hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3848990
hg1948990
hg1848990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021328, nsv1021868
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)dgv6618n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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