A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17503936



Internal ID22561879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131058276..131067826hg38UCSC Ensembl
chr7:130743035..130752585hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg389551
hg199551
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864152
Supporting Variants
Samples
Known GenesLINC-PINT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17503936
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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