A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500612



Internal ID20873840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78086312..78093688hg38UCSC Ensembl
chr15:78378654..78386030hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387377
hg197377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026752
Samples
Known GenesSH2D7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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