A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140409



Internal ID21507513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32097934..32098243hg38UCSC Ensembl
chr7:32137546..32137855hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579587
Supporting Variants
SamplesNA19983
Known GenesPDE1C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140409
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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