A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007690



Internal ID19096909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113853968..113901765hg38UCSC Ensembl
Innerchr3:113572815..113620612hg19UCSC Ensembl
Innerchr3:115055505..115103302hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3847798
hg1947798
hg1847798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4841n100
Supporting Variantsnssv3735266, nssv3604463, nssv3604462
Samples
Known GenesGRAMD1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007690
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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