A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985098



Internal ID19222823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:157005006..157005506hg38UCSC Ensembl
Outerchr7:156797700..156798200hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126822
Supporting Variants
SamplesKWS1
Known GenesMNX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985098
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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