A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500669



Internal ID20873897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10356456..10570652hg38UCSC Ensembl
chr16:10450313..10664509hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38214197
hg19214197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028268
Samples
Known GenesATF7IP2, EMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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