A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075870



Internal ID21415505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7432559..7432633hg38UCSC Ensembl
chr11:7453790..7453864hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600475
Supporting Variants
SamplesHG00731
Known GenesSYT9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075870
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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