A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007359



Internal ID19096578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7726973..8302289hg38UCSC Ensembl
Innerchr3:7768660..8343977hg19UCSC Ensembl
Innerchr3:7743660..8318977hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38575317
hg19575318
hg18575318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591835, nssv3591836
Samples
Known GenesGRM7, LMCD1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007359
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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