A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620597



Internal ID18572192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25362237..25915432hg38UCSC Ensembl
Innerchr4:25363859..25917054hg19UCSC Ensembl
Innerchr4:24972957..25526152hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38553196
hg19553196
hg18553196
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997544
Supporting Variants
Samples
Known GenesANAPC4, SEL1L3, SLC34A2, SMIM20, ZCCHC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3620597
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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