A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv215e55



Internal ID20126694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31391844..31506911hg38UCSC Ensembl
chr6:31359621..31474688hg19UCSC Ensembl
chr6:31467600..31582667hg18UCSC Ensembl
chr6:31467600..31582667hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38115068
hg19115068
hg18115068
hg17115068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv35005, esv34619, esv34376, esv34991, esv34684, esv2752121, esv34950, esv34444
SamplesNA18969, NA15510, NA18563, SPC_162, NA18620, NA18558, NA19201, NA19202
Known GenesHCG26, HCP5, MICA, MICB
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv215e55
Frequency
Sample Size771
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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