A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152618



Internal ID15855026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7182257..7220635hg38UCSC Ensembl
Innerchr4:7183984..7222362hg19UCSC Ensembl
Innerchr4:7234885..7273263hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3838379
hg1938379
hg1838379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593563
Supporting Variants
Samples1780862416_A
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152618
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