A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv465244



Internal ID15525309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155181214..155187164hg38UCSC Ensembl
Innerchr7:154972924..154978874hg19UCSC Ensembl
Innerchr7:154603857..154609807hg18UCSC Ensembl
Innerchr7:154410572..154416522hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385951
hg195951
hg185951
hg175951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv541080
SamplesHGDP01053
Known Genes
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)nsv465244
Frequency
Sample Size1557
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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