A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6090n100



Internal ID22792177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91271156..91420431hg38UCSC Ensembl
chr6:91980874..92130149hg19UCSC Ensembl
chr6:92037595..92186870hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38149276
hg19149276
hg18149276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030361, nsv1025794, nsv1020313
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)dgv6090n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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