A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096483



Internal ID15949669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:142878270..142884980hg38UCSC Ensembl
Innerchr7:142576015..142582725hg19UCSC Ensembl
Innerchr7:142286137..142292847hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386711
hg196711
hg186711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608656
Supporting Variants
Samples
Known GenesTRPV6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1096483
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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