A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020524



Internal ID19109743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101369721..101473041hg38UCSC Ensembl
Innerchr7:101013002..101116322hg19UCSC Ensembl
Innerchr7:100799722..100903042hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38103321
hg19103321
hg18103321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656102
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020524
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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