A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155106



Internal ID15507773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1388817..1554022hg38UCSC Ensembl
Innerchr7:1428453..1593658hg19UCSC Ensembl
Innerchr7:1394979..1560184hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38165206
hg19165206
hg18165206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605815
Supporting Variants
Samples1780862127_A
Known GenesINTS1, MAFK, MICALL2, TMEM184A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155106
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