A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6603n100



Internal ID22792690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122173126..122259649hg38UCSC Ensembl
chr7:121813180..121899703hg19UCSC Ensembl
chr7:121600416..121686939hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3886524
hg1986524
hg1886524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034797, nsv1034624, nsv1028221, nsv1024868
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)dgv6603n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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