A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141877



Internal ID341076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75116779..75158779hg38UCSC Ensembl
chr7:74532588..74574585hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3842001
hg1941998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001062
Samples
Known GenesGTF2IRD2, GTF2IRD2B, NCF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141877
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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