A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021638



Internal ID19110856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..7148455hg38UCSC Ensembl
Innerchr7:6854098..7188086hg19UCSC Ensembl
Innerchr7:6820623..7154611hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38333989
hg19333989
hg18333989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6245n100
Supporting Variantsnssv3752813
Samples
Known GenesCCZ1B, LOC100131257
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021638
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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