A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608150



Internal ID16395559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110677971..110814300hg38UCSC Ensembl
Innerchr7:110318027..110454356hg19UCSC Ensembl
Innerchr7:110105263..110241592hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38136330
hg19136330
hg18136330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155371
Samples1798860072_A
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608150
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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