A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024458



Internal ID18766990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:30562261..30610043hg38UCSC Ensembl
Innerchr7:30601877..30649659hg19UCSC Ensembl
Innerchr7:30568402..30616184hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3847783
hg1947783
hg1847783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643350
Samples
Known GenesGARS, LOC401320
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024458
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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