A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026491



Internal ID19115709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35680650..35756755hg38UCSC Ensembl
Innerchr7:35720260..35796365hg19UCSC Ensembl
Innerchr7:35686785..35762890hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3876106
hg1976106
hg1876106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643408
Samples
Known GenesHERPUD2, LOC100506725
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026491
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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