A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603253



Internal ID20976324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123695701..123697600hg38UCSC Ensembl
chr7:123335755..123337654hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150098
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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