A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv658n27



Internal ID22767387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67931662..68011858hg38UCSC Ensembl
chr4:68797380..68877576hg19UCSC Ensembl
chr4:68479975..68560171hg18UCSC Ensembl
chr4:68626146..68706342hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3880197
hg1980197
hg1880197
hg1780197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv461542, nsv461543, nsv461544, nsv461545
SamplesHGDP00285, HGDP00315, HGDP00333, HGDP00313
Known GenesTMPRSS11A, TMPRSS11GP
MethodSNP array
AnalysisAn HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives.
PlatformNot reported
Comments
ReferenceItsara_et_al_2009
Pubmed ID19166990
Accession Number(s)dgv658n27
Frequency
Sample Size1557
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer