A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001751



Internal ID19090968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:123772191..123812150hg38UCSC Ensembl
Innerchr4:124693346..124733305hg19UCSC Ensembl
Innerchr4:124912796..124952755hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3839960
hg1939960
hg1839960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3743092
Samples
Known GenesLINC01091
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001751
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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