A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999023



Internal ID19158559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61873956..61919203hg38UCSC Ensembl
Innerchr4:62739674..62784921hg19UCSC Ensembl
Innerchr4:62422269..62467516hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3845248
hg1945248
hg1845248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626518
Samples
Known GenesLPHN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999023
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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