A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3864n100



Internal ID22789951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71364462..71408004hg38UCSC Ensembl
chr2:71591592..71635134hg19UCSC Ensembl
chr2:71445100..71488642hg18UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3843543
hg1943543
hg1843543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002965, nsv997841
Samples
Known GenesZNF638
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3864n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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