A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032108



Internal ID19121330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126638295..126722538hg38UCSC Ensembl
Innerchr7:126278349..126362592hg19UCSC Ensembl
Innerchr7:126065585..126149828hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3884244
hg1984244
hg1884244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751539
Samples
Known GenesGRM8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032108
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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