A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032640



Internal ID19121862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143790559..143875193hg38UCSC Ensembl
Innerchr7:143487652..143572286hg19UCSC Ensembl
Innerchr7:143118585..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3884635
hg1984635
hg1884635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6722n100
Supporting Variantsnssv3671134, nssv3671135
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032640
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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