A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3628903



Internal ID18927184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569882..68620249hg38UCSC Ensembl
Innerchr4:69435600..69485967hg19UCSC Ensembl
Innerchr4:69118195..69168562hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3850368
hg1950368
hg1850368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010832
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3628903
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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