A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6619n100



Internal ID22792706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131347777..131422147hg38UCSC Ensembl
chr7:131032536..131106906hg19UCSC Ensembl
chr7:130683076..130757446hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3874371
hg1974371
hg1874371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032787, nsv1025264
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)dgv6619n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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