A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032623



Internal ID19121845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136850192hg38UCSC Ensembl
Innerchr8:137687873..137862435hg19UCSC Ensembl
Innerchr8:137757055..137931617hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38174563
hg19174563
hg18174563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690013, nssv3690007, nssv3690014, nssv3757489, nssv3690005, nssv3690019, nssv3690018, nssv3690020, nssv3757487, nssv3690023, nssv3690022, nssv3690024, nssv3757488, nssv3690009, nssv3690008, nssv3690017, nssv3690015, nssv3690004, nssv3757490, nssv3690016, nssv3690012, nssv3690010, nssv3690011, nssv3690006, nssv3690021
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032623
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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