A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658903



Internal ID15395555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111337288..111389508hg38UCSC Ensembl
Innerchr7:110977344..111029564hg19UCSC Ensembl
Innerchr7:110764580..110816800hg18UCSC Ensembl
Innerchr7:110571295..110623515hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3852221
hg1952221
hg1852221
hg1752221
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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