A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv988539



Internal ID15935809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2253738..2262338hg38UCSC Ensembl
Innerchr4:2255465..2264065hg19UCSC Ensembl
Innerchr4:2225263..2233863hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388601
hg198601
hg188601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593383
Supporting Variants
Samples
Known GenesMXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv988539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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