A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560661



Internal ID21885016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41700779..41700876hg38UCSC Ensembl
chr7:41740377..41740474hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018963
Supporting Variants
Samples
Known GenesINHBA, INHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560661
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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