A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695149



Internal ID15431801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7825097..7830250hg38UCSC Ensembl
Innerchr4:7826824..7831977hg19UCSC Ensembl
Innerchr4:7877724..7882877hg18UCSC Ensembl
Innerchr4:7944895..7950048hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg385154
hg195154
hg185154
hg175154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522369
Supporting Variants
Samples
Known GenesAFAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695149
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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