A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1n35



Internal ID22767744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91387226..91387226hg38UCSC Ensembl
chr1:91852783..91852783hg19UCSC Ensembl
chr1:91625371..91625371hg18UCSC Ensembl
chr1:91564804..91564804hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv477339, nsv481561, nsv473786
SamplesNA12156, NA18517
Known GenesHFM1
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
Comments
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)dgv1n35
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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