A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156026



Internal ID15878660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137140775..137198178hg38UCSC Ensembl
Innerchr7:136825522..136882925hg19UCSC Ensembl
Innerchr7:136476062..136533465hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3857404
hg1957404
hg1857404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608463
Supporting Variants
SamplesHGDP01238
Known GenesLOC349160
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156026
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