A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155791



Internal ID15878877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148889954..148920959hg38UCSC Ensembl
Innerchr6:149211090..149242095hg19UCSC Ensembl
Innerchr6:149252783..149283788hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3831006
hg1931006
hg1831006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604844
Supporting Variants
SamplesHGDP01272
Known GenesUST
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155791
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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