A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998622



Internal ID17291574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:150326212..150342411hg38UCSC Ensembl
Outerchr7:150023301..150039500hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951645
Supporting Variants
SamplesBILGI_BIOE
Known GenesLRRC61, RARRES2, ZBED6CL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998622
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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