A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896611



Internal ID171885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16483139..16940239hg38UCSC Ensembl
chr1:16809634..17266734hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38457101
hg19457101
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560911
Supporting Variants
Samples
Known GenesCROCC, CROCCP2, CROCCP3, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896611
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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