A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026055



Internal ID19115272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13054314..13090444hg38UCSC Ensembl
Innerchr7:13093939..13130069hg19UCSC Ensembl
Innerchr7:13060464..13096594hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836131
hg1936131
hg1836131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6277n100
Supporting Variantsnssv3643029, nssv3643016, nssv3643015, nssv3643014, nssv3643021, nssv3643009, nssv3643011, nssv3643005, nssv3643018, nssv3643017, nssv3643008, nssv3643020, nssv3643024, nssv3643013, nssv3643003, nssv3643019, nssv3643006, nssv3643026, nssv3643027, nssv3643007, nssv3643023, nssv3643004, nssv3643002, nssv3643025, nssv3643012, nssv3643022, nssv3643030, nssv3643028, nssv3643010
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)nsv1026055
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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