A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6243n100



Internal ID20157859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5828930..5931291hg38UCSC Ensembl
chr7:5868561..5970922hg19UCSC Ensembl
chr7:5835087..5937448hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38102362
hg19102362
hg18102362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026461, nsv1031583, nsv1024675
Samples
Known GenesCCZ1, OCM, RSPH10B, RSPH10B2, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6243n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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