A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025570



Internal ID19114788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:97756249..97775799hg38UCSC Ensembl
Innerchr7:97385561..97405111hg19UCSC Ensembl
Innerchr7:97223497..97243047hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3819551
hg1919551
hg1819551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755447
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)nsv1025570
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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