A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610929



Internal ID20984000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94631568..94632033hg38UCSC Ensembl
chr7:94260880..94261345hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161539
Samples
Known GenesSGCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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