A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6766n100



Internal ID22792853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155263004..155284018hg38UCSC Ensembl
chr7:155054714..155075728hg19UCSC Ensembl
chr7:154685647..154706661hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3821015
hg1921015
hg1821015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034420, nsv1019278, nsv1024528
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6766n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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