A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244002



Internal ID21305367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99410900..99556305hg38UCSC Ensembl
Outerchr4:99410515..99561532hg38UCSC Ensembl
Innerchr4:100332057..100477462hg19UCSC Ensembl
Outerchr4:100331672..100482689hg19UCSC Ensembl
Innerchr4:100551080..100696485hg18UCSC Ensembl
Outerchr4:100550695..100701712hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38151018
hg19151018
hg18151018
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169903
Supporting Variants
SamplesNGO_20
Known GenesADH7, C4orf17, TRMT10A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244002
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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