A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6524n100



Internal ID22792611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88503095..88627862hg38UCSC Ensembl
chr7:88132410..88257176hg19UCSC Ensembl
chr7:87970346..88095112hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38124768
hg19124767
hg18124767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030170, nsv1017090, nsv1023360, nsv1018761, nsv1034941
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)dgv6524n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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