A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998620



Internal ID17291572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:149768812..149833811hg38UCSC Ensembl
Outerchr7:149465901..149530900hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3865000
hg1965000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951643
Supporting Variants
SamplesBILGI_BIOE
Known GenesSSPO, ZNF467
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998620
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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