A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7171n100



Internal ID22793258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39372794..39499344hg38UCSC Ensembl
chr8:39230313..39356863hg19UCSC Ensembl
chr8:39349470..39476020hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38126551
hg19126551
hg18126551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015405, nsv1021742, nsv1027662, nsv1018476, nsv1025473, nsv1026810
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7171n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss105
Observed Complex0
Frequencyn/a


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