A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142485



Internal ID341685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139497673..139531753hg38UCSC Ensembl
chr7:139182419..139216499hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3834081
hg1934081
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003742
Samples
Known GenesCLEC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142485
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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