A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997695



Internal ID18810545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7534576..7714630hg38UCSC Ensembl
Innerchr3:7576263..7756317hg19UCSC Ensembl
Innerchr3:7551263..7731317hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38180055
hg19180055
hg18180055
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739588
Samples
Known GenesGRM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997695
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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