A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515347



Internal ID20888706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30716660..30717892hg38UCSC Ensembl
chr16:30727981..30729213hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381233
hg191233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029179
Samples
Known GenesSRCAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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