A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156552



Internal ID15879707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99157649..99190966hg38UCSC Ensembl
Innerchr7:98755272..98788589hg19UCSC Ensembl
Innerchr7:98593208..98626525hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3833318
hg1933318
hg1833318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607925
Supporting Variants
SamplesHGDP01418
Known GenesKPNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156552
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