A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607728



Internal ID20980799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36413503..36414853hg38UCSC Ensembl
chr7:36453112..36454462hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381351
hg191351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153733
Samples
Known GenesANLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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