A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3631005



Internal ID18582600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99196119..99523288hg38UCSC Ensembl
Innerchr4:100117276..100444445hg19UCSC Ensembl
Innerchr4:100336299..100663468hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38327170
hg19327170
hg18327170
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000659
Supporting Variants
Samples
Known GenesADH1A, ADH1B, ADH1C, ADH6, ADH7, C4orf17, LOC100507053
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3631005
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer