A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2641n100



Internal ID19013009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84153209..84546378hg38UCSC Ensembl
chr15:84821961..85089609hg19UCSC Ensembl
chr15:82612965..82890613hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38393170
hg19267649
hg18277649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035348, nsv1049804, nsv1053457, nsv1042566, nsv1045541
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC100505679, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2641n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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