A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462604



Internal ID21120157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71587217..71887226hg38UCSC Ensembl
chr11:71298263..71598272hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38300010
hg19300010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992881
Samples
Known GenesALG1L9P, DEFB108B, FAM86C1, LOC100129216, LOC100133315, ZNF705E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer