A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004634



Internal ID19093851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43184487..43211021hg38UCSC Ensembl
Innerchr4:43186504..43213038hg19UCSC Ensembl
Innerchr4:42881261..42907795hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3826535
hg1926535
hg1826535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5197n100
Supporting Variantsnssv3625050
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)nsv1004634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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