A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999894



Internal ID17292846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:56661033..56671732hg38UCSC Ensembl
Outerchr19:57172401..57183100hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952152
Supporting Variants
SamplesBILGI_BIOE
Known GenesZNF835
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999894
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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