A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005129



Internal ID16951395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:61924935..61925284hg38UCSC Ensembl
Outerchr1:62390607..62390956hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv958705
Supporting Variants
SamplesBILGI_BIOE
Known GenesINADL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005129
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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