A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092682



Internal ID15599182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110651990..110977789hg38UCSC Ensembl
Innerchr7:110292046..110617845hg19UCSC Ensembl
Innerchr7:110079282..110405081hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38325800
hg19325800
hg18325800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608147
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092682
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