A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425369



Internal ID21082922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127821874..127954174hg38UCSC Ensembl
chr7:127461927..127594227hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38132301
hg19132301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152698
Samples
Known GenesSND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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