A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025437



Internal ID19114655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:14187116..14256046hg38UCSC Ensembl
Innerchr7:14226741..14295671hg19UCSC Ensembl
Innerchr7:14193266..14262196hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3868931
hg1968931
hg1868931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643154, nssv3643155
Samples
Known GenesDGKB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025437
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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