A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025799



Internal ID19115016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81140765..81189433hg38UCSC Ensembl
Innerchr5:80436584..80485252hg19UCSC Ensembl
Innerchr5:80472340..80521008hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3848669
hg1948669
hg1848669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639134, nssv3639135
Samples
Known GenesRASGRF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025799
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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