A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6564n100



Internal ID20158180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110589001..110749639hg38UCSC Ensembl
chr7:110229058..110389695hg19UCSC Ensembl
chr7:110016294..110176931hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38160639
hg19160638
hg18160638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026955, nsv1023334, nsv1021897
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6564n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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