A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1082499



Internal ID15935685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550861..31551943hg38UCSC Ensembl
Innerchr7:31590475..31591557hg19UCSC Ensembl
Innerchr7:31557000..31558082hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381083
hg191083
hg181083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606566
Supporting Variants
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1082499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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