A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143999



Internal ID21438885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77014959..77042880hg38UCSC Ensembl
chr7:76644276..76672197hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3827922
hg1927922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583044
Supporting Variants
SamplesHG00732
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143999
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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