A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032126



Internal ID19121348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19052837..19097605hg38UCSC Ensembl
Innerchr7:19092460..19137228hg19UCSC Ensembl
Innerchr7:19058985..19103753hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3844769
hg1944769
hg1844769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6299n100
Supporting Variantsnssv3643239
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)nsv1032126
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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