A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625003



Internal ID18923284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35369560..35420431hg38UCSC Ensembl
Innerchr4:35371182..35422053hg19UCSC Ensembl
Innerchr4:35047577..35098448hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3850872
hg1950872
hg1850872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998061
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)nssv3625003
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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