A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572884



Internal ID21764927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71387214..71387277hg38UCSC Ensembl
chr7:70852200..70852263hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017821
Supporting Variants
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572884
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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